Emission II: Collisional & Photoionized Plasmas
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HI Balmer Jump Temperatures for Extragalactic HII Regions in the CHAOS Galaxies
HI Balmer Jump Temperatures for Extragalactic HII Regions in the CHAOS Galaxies A Senior Thesis Presented in Partial Fulfillment of the Requirements for Graduation with Research Distinction in Astronomy in the Undergraduate Colleges of The Ohio State University By Ness Mayker The Ohio State University April 2019 Project Advisors: Danielle A. Berg, Richard W. Pogge Table of Contents Chapter 1: Introduction ............................... 3 1.1 Measuring Nebular Abundances . 8 1.2 The Balmer Continuum . 13 Chapter 2: Balmer Jump Temperature in the CHAOS galaxies .... 16 2.1 Data . 16 2.1.1 The CHAOS Survey . 16 2.1.2 CHAOS Balmer Jump Sample . 17 2.2 Balmer Jump Temperature Determinations . 20 2.2.1 Balmer Continuum Significance . 20 2.2.2 Balmer Continuum Measurements . 21 + 2.2.3 Te(H ) Calculations . 23 2.2.4 Photoionization Models . 24 2.3 Results . 26 2.3.1 Te Te Relationships . 26 − 2.3.2 Discussion . 28 Chapter 3: Conclusions and Future Work ................... 32 1 Abstract By understanding the observed proportions of the elements found across galaxies astronomers can learn about the evolution of life and the universe. Historically, there have been consistent discrepancies found between the two main methods used to measure gas-phase elemental abundances: collisionally excited lines and optical recombination lines in H II regions (ionized nebulae around young star-forming regions). The origin of the discrepancy is thought to hinge primarily on the strong temperature dependence of the collisionally excited emission lines of metal ions, principally Oxygen, Nitrogen, and Sulfur. This problem is exacerbated by the difficulty of measuring ionic temperatures from these species. -
1.1 Questions Chapter 1
i 1.1 Questions Chapter 1 Question 1.5 Question 1.5 What is H I? And H II and H III? Do these spectra have spectral lines? What is the 21 cm line associated with? Does Fe XII have spectral lines? If so, in which wavelength region? H I = the spectrum of neutral hydrogen (proton + electron). H II = the spectrum of ionized hydrogen (H+, free proton). H III does not exist. H I contains the Lyman-, Balmer-, Paschen-, Pfundt- etc. series, see Figure 1.4 H II does not have spectral lines, there is no bound electron that can do bb transi- tions. The 21 cm line is part of the H I spectrum but is not part of a series of bb transitions of the electron; this transition is a flip of the spin of the electron in the ground state. The energy difference between these two spin states is ∆Espin = 6 × 10−6 eV. Fe XII is the spectrum of Fe11+. This spectrum contains lines because the twelfth, thirteenth electron, etc. still can make bb transitions. These inner-shell electrons are strongly bound, therefore the ∆Emn is large and the spectral lines have short wavelengths. Figure 8.11 shows an example of the emission line of Fe XII at 195 A.˚ Question 1.6 Question 1.6 Compare the observed wavelengths of the Na I D lines in Figure 1.2 and the Lyα line in Figure 1.3 with those of the associated bb transitions in the relevant term diagrams (see Appendix). What is your conclusion? Figure 1.3 shows a large number of spectral lines with λ < 3530 A:˚ the Lyα forest. -
Resonance Raman Scattering of Light from a Diatomic Molecule
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Electrical & Computer Engineering, Department P. F. (Paul Frazer) Williams Publications of May 1976 Resonance Raman scattering of light from a diatomic molecule D. L. Rousseau Bell Laboratories, Murray Hill, New Jersey P. F. Williams University of Nebraska - Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/elecengwilliams Part of the Electrical and Computer Engineering Commons Rousseau, D. L. and Williams, P. F., "Resonance Raman scattering of light from a diatomic molecule" (1976). P. F. (Paul Frazer) Williams Publications. 24. https://digitalcommons.unl.edu/elecengwilliams/24 This Article is brought to you for free and open access by the Electrical & Computer Engineering, Department of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in P. F. (Paul Frazer) Williams Publications by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Resonance Raman scattering of light from a diatomic molecule D. L. Rousseau Bell Laboratories. Murray Hill, New Jersey 07974 P. F. Williams Bell Laboratories, Murray Hill, New Jersey 07974 and Department of Physics, University of Puerto Rico, Rio Piedras, Puerto Rico 00931 (Received 13 October 1975) Resonance Raman scattering from a homonuclear diatomic molecule is considered in detail. For convenience, the scattering may be classified into three excitation frequency regions-off-resonance Raman scattering for inciderit energies well away from resonance with any allowed transitions, discrete resonance Raman scattering for excitation near or in resonance with discrete transitions, and continuum resonance Raman scattering for excitation resonant with continuum transitions, e.g., excitation above a dissociation limit or into a repulsive electronic state. -
E R U P T I V E S T a R S S P E C T R O S C O
Erupti ve stars spectroscopy Catacl ys mics, Sy mbi otics, Novae, Supernovae ARAS Eruptive Stars Information letter n° 14 #2015‐02 28‐02‐2015 Observations of February 2015 Contents News Two novae discovered in february Novae p. 2‐8 Nova Sco 2015 = PNV J17032620‐3504140 Nova Cyg 2014 Nova Cen 2013 Ungoing observations 2015 February 11.837 UT at mag 8.1 Nova Del 2013 rsising in the morning sky by Tadashi Kojima Nova Sco 2015 Nova Sgr 2015 Spectra obtained by C. Buil Nova Sgr 2015 = PNV J18142514‐2554343 Symbiotics p. 9‐22 2015 February 12.840 at mag 11.2 by Hideo Nishimura, Survey of V694 Mon Koichi Nishiyama CH Cygni campaign : fisrt spectrum of the new season the 1th of and Fujio Kabashima march ( see next issue) Cataclysmics p. 23‐27 SS Aur in outburst : a complete coverage of the outburst in February by P. Somgogyi and J. Guarro U Gem outburst late February Notes from Steve shore : p. 28‐31 Recent publications about eruptive stars p. 32‐34 ARAS Spectroscopy Extra : Cat’s eye nebula spectroscopy, 150 years after Huggins, ARAS Web page by Olivier Thizy http://www.astrosurf.com/aras/ p. 35 ‐ 47 ARAS Forum http://www.spectro‐aras.com/forum/ ARAS list https://groups.yahoo.com/neo/groups/sp Acknowledgements : ectro‐l/info V band light curves from AAVSO photometric data base ARAS preliminary data base http://www.astrosurf.com/aras/Aras_Data Authors : Base/DataBase.htm F. Teyssier, S. Shore, A. Skopal, P. Somogyi, D. Boyd, J. Edlin, J. Guarro, ARAS BeAM Franck Boubault http://arasbeam.free.fr/?lang=en ARAS Eruptive Stars Information Letter -
Atomic Excitation Potentials
ATOMIC EXCITATION POTENTIALS PURPOSE In this lab you will study the excitation of mercury atoms by colliding electrons with the atoms, and confirm that this excitation requires a specific quantity of energy. THEORY In general, atoms of an element can exist in a number of either excited or ionized states, or the ground state. This lab will focus on electron collisions in which a free electron gives up just the amount of kinetic energy required to excite a ground state mercury atom into its first excited state. However, it is important to consider all other processes which constantly change the energy states of the atoms. An atom in the ground state may absorb a photon of energy exactly equal to the energy difference between the ground state and some excited state, whereas another atom may collide with an electron and absorb some fraction of the electron's kinetic energy which is the amount needed to put that atom in some excited state (collisional excitation). Each atom in an excited state then spontaneously emits a photon and drops from a higher excited state to a lower one (or to the ground state). Another possibility is that an atom may collide with an electron which carries away kinetic energy equal to the atomic excitation energy so that the atom ends up in, say, the ground state (collisional deexcitation). Lastly, an atom can be placed into an ionized state (one or more of its electrons stripped away) if the collision transfers energy greater than the ionization potential of the atom. Likewise an ionized atom can capture a free electron. -
Raman Spectroscopy for In-Line Water Quality Monitoring — Instrumentation and Potential
Sensors 2014, 14, 17275-17303; doi:10.3390/s140917275 OPEN ACCESS sensors ISSN 1424-8220 www.mdpi.com/journal/sensors Review Raman Spectroscopy for In-Line Water Quality Monitoring — Instrumentation and Potential Zhiyun Li 1, M. Jamal Deen 1,2,4,*, Shiva Kumar 2 and P. Ravi Selvaganapathy 1,3 1 School of Biomedical Engineering, McMaster University, Hamilton, ON L8S 4K1, Canada; E-Mails: [email protected] (Z.L.); [email protected] (P.R.S.) 2 Electrical and Computer Engineering, McMaster University, Hamilton, ON L8S 4K1 Canada; E-Mail: [email protected] 3 Mechanical Engineering, McMaster University, Hamilton, ON L8S 4K1, Canada 4 Electronic and Computer Engineering, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China * Author to whom correspondence should be addressed; E-Mail: [email protected] or [email protected]; Tel.: +1-905-525-9140 (ext. 27137); Fax: +1-905-521-2922. Received: 1 July 2014; in revised form: 7 September 2014 / Accepted: 9 September 2014 / Published: 16 September 2014 Abstract: Worldwide, the access to safe drinking water is a huge problem. In fact, the number of persons without safe drinking water is increasing, even though it is an essential ingredient for human health and development. The enormity of the problem also makes it a critical environmental and public health issue. Therefore, there is a critical need for easy-to-use, compact and sensitive techniques for water quality monitoring. Raman spectroscopy has been a very powerful technique to characterize chemical composition and has been applied to many areas, including chemistry, food, material science or pharmaceuticals. -
Basics of Plasma Spectroscopy
Home Search Collections Journals About Contact us My IOPscience Basics of plasma spectroscopy This content has been downloaded from IOPscience. Please scroll down to see the full text. 2006 Plasma Sources Sci. Technol. 15 S137 (http://iopscience.iop.org/0963-0252/15/4/S01) View the table of contents for this issue, or go to the journal homepage for more Download details: IP Address: 198.35.1.48 This content was downloaded on 20/06/2014 at 16:07 Please note that terms and conditions apply. INSTITUTE OF PHYSICS PUBLISHING PLASMA SOURCES SCIENCE AND TECHNOLOGY Plasma Sources Sci. Technol. 15 (2006) S137–S147 doi:10.1088/0963-0252/15/4/S01 Basics of plasma spectroscopy U Fantz Max-Planck-Institut fur¨ Plasmaphysik, EURATOM Association Boltzmannstr. 2, D-85748 Garching, Germany E-mail: [email protected] Received 11 November 2005, in final form 23 March 2006 Published 6 October 2006 Online at stacks.iop.org/PSST/15/S137 Abstract These lecture notes are intended to give an introductory course on plasma spectroscopy. Focusing on emission spectroscopy, the underlying principles of atomic and molecular spectroscopy in low temperature plasmas are explained. This includes choice of the proper equipment and the calibration procedure. Based on population models, the evaluation of spectra and their information content is described. Several common diagnostic methods are presented, ready for direct application by the reader, to obtain a multitude of plasma parameters by plasma spectroscopy. 1. Introduction spectroscopy for purposes of chemical analysis are described in [11–14]. Plasma spectroscopy is one of the most established and oldest diagnostic tools in astrophysics and plasma physics 2. -
Fluorescent, Prussian Blue-Based Biocompatible Nanoparticle System for Multimodal Imaging Contrast
Supplementary Materials Fluorescent, Prussian Blue-Based Biocompatible Nanoparticle System for Multimodal Imaging Contrast László Forgách 1,*, Nikolett Hegedűs 1, Ildikó Horváth 1, Bálint Kiss 1, Noémi Kovács 1, Zoltán Varga 1,2, Géza Jakab 3, Tibor Kovács 4, Parasuraman Padmanabhan 5, Krisztián Szigeti 1,*,† and Domokos Máthé 1,6,7,*,† 1 Department of Biophysics and Radiation Biology, Semmelweis University, 1085 Budapest, Hungary; [email protected] (N.H.); [email protected] (I.H.); [email protected] (B.K.); [email protected] (N.K.); [email protected] (Z.V.) 2 Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, 1117 Budapest, Hungary; [email protected] (Z.V.) 3 Department of Pharmaceutics, Semmelweis University, 1085 Budapest, Hungary; [email protected] 4 University of Pannonia, Institute of Radiochemistry and Radioecology, 8200 Veszprém, Hungary; [email protected] 5 Lee Kong Chian School of Medicine, Nanyang Technological University, 636921 Singapore, Singapore; [email protected] 6 In Vivo Imaging Advanced Core Facility, Hungarian Centre of Excellence for Molecular Medicine, 6723 Szeged, Hungary 7 CROmed Translational Research Centers, 1047 Budapest, Hungary * Correspondence: [email protected] (L.F.); [email protected] univ.hu (K.S.); [email protected] (D.M.); Tel.: +36-1-459-1500/60164 (L.F.); +36-1- 459-1500/60210 (D.M.) † These authors contributed equally to this work. Native, citrate-coated PBNPs The mean hydrodynamic diameter (intensity-based harmonic means or z-average) of citrate- coated PBNPs was 29.30 ± 2.08 (average ± SD, 푛 = 8), as determined by DLS. -
Arxiv:1012.0600V1 [Astro-Ph.SR] 2 Dec 2010 a Ulctossre,Vl ,2018 Publisher ?, the Vol
Title : will be set by the publisher Editors : will be set by the publisher EAS Publications Series, Vol. ?, 2018 NON-LTE MODEL ATOM CONSTRUCTION Norbert Przybilla1 Abstract. Model atoms are an integral part in the solution of non- LTE problems. They comprise the atomic input data that are used to specify the statistical equilibrium equations and the opacities and emissivities of radiative transfer. A realistic implementation of the structure and the processes governing the quantum-mechanical system of an atom is decisive for the successful modelling of observed spectra. We provide guidelines and suggestions for the construction of robust and comprehensive model atoms as required in non-LTE line-formation computations for stellar atmospheres. Emphasis is given on the use of standard stars for testing model atoms under a wide range of plasma conditions. 1 Introduction Astrophysical plasmas like stellar atmospheres, gaseous nebulae or accretion disks are not in any sense closed systems, as they emit photons into interstellar space. Therefore, the thermodynamic state of such plasmas is in general not described well by the equilibrium relations of statistical mechanics and thermodynamics for local values of temperature and density, i.e. by local thermodynamic equilibrium (LTE). The presence of an intense radiation field, which in character is very dif- ferent from the equilibrium Planck distribution, results in deviations from LTE (non-LTE) because of strong interactions between photons and particles. The thermodynamic state is then determined by the principle of statistical equilib- rium. All microscopic processes that produce transitions from one atomic state arXiv:1012.0600v1 [astro-ph.SR] 2 Dec 2010 to another need to be considered in detail via the rate equations. -
Ice Features in the Mid-IR Spectra of Galactic Nuclei?
A&A 385, 1022–1041 (2002) Astronomy DOI: 10.1051/0004-6361:20020147 & c ESO 2002 Astrophysics Ice features in the mid-IR spectra of galactic nuclei? H. W. W. Spoon1,2,J.V.Keane2,A.G.G.M.Tielens2,3,D.Lutz4,A.F.M.Moorwood1, and O. Laurent4 1 European Southern Observatory, Karl-Schwarzschild-Strasse 2, 85748 Garching, Germany e-mail: [email protected]; [email protected] 2 Kapteyn Institute, PO Box 800, 9700 AV Groningen, The Netherlands e-mail: [email protected]; [email protected] 3 SRON, PO Box 800, 9700 AV Groningen, The Netherlands 4 Max-Planck-Institut f¨ur Extraterrestrische Physik (MPE), Postfach 1312, 85741 Garching, Germany e-mail: [email protected] Received 28 November 2001 / Accepted 24 January 2002 Abstract. Mid infrared spectra provide a powerful probe of the conditions in dusty galactic nuclei. They variously contain emission features associated with star forming regions and absorptions by circumnuclear silicate dust plus ices in cold molecular cloud material. Here we report the detection of 6–8 µm water ice absorption in 18 galaxies observed by ISO. While the mid-IR spectra of some of these galaxies show a strong resemblance to the heavily absorbed spectrum of NGC 4418, other galaxies in this sample also show weak to strong PAH emission. The 18 ice galaxies are part of a sample of 103 galaxies with good S/N mid-IR ISO spectra. Based on our sample we find that ice is present in most of the ULIRGs, whereas it is weak or absent in the large majority of Seyferts and starburst galaxies. -
2.7.6 Excitation-Autoionisation in the Previous Section We Showed How a Collision of a Free Electron with an Ion Can Lead to Ionisation
2.7.6 Excitation-Autoionisation In the previous section we showed how a collision of a free electron with an ion can lead to ionisation. In principle, if the free electron has insufficient energy (E<I), there will be no ionisation. However, even in that case it is sometimes possible to ionise, but in a more complicated way. The process is as follows. The collision can bring one of the electrons in the outermost shells in a higher quantum level (excitation). In most cases, the ion will return to its ground level by a radiative transition. But in some cases the excited state is unstable, and a radiationless Auger transition can occur. Later on we will treat the Auger process in more detail, but shortly speaking the vacancy that is left behind by the excited electron is being filled by another electron from one of the outermost shells, while the excited electron is able to leave the ion (or a similar, process with the role of both electrons reversed). Because of energy conservation, this process only occurs if the excited electron comes from one of the inner shells (the ionisation potential barrier must be taken anyhow). The process is in particular important for Li-like and Na-like ions, and for several other individual atoms and ions. Figure 2.16: The Excitation-Autoionisation process for a Li-like ion. As an example we treat here Li-like ions (see Fig. 2.16). In that case the most important contribution comes from a 1s–2p excitation. The effective cross section Q for excitation from 1s to 2p followed by auto-ionisation can be approximated by (EH = 13.6 eV): 2 2 Z EH Q = πa0 2B 2 ΩH (2.38) Zeff (1s) E in which a0 is the Bohr radius, and Zeff = Z 0.43 is the effective charge that a 1s electron experiences because of the presence− of the other 1s electron and the 2s electron in the Li-like ion. -
Molecular Excitation in the Interstellar Medium: Recent Advances In
Molecular excitation in the Interstellar Medium: recent advances in collisional, radiative and chemical processes Evelyne Roueff∗,† and François Lique∗,‡ Laboratoire Univers et Théories, Observatoire de Paris, 92190, Meudon, France, and LOMC - UMR 6294, CNRS-Université du Havre, 25 rue Philippe Lebon, BP 540, 76058, Le Havre, France E-mail: [email protected]; [email protected] Contents 1 Introduction 3 2 Collisional excitation 7 2.1 Methods . 9 2.1.1 Theory . 9 2.1.2 Potential energy surfaces . 10 2.1.3 Scattering Calculations . 13 arXiv:1310.8259v1 [physics.chem-ph] 30 Oct 2013 2.1.4 Experiments . 17 2.2 H2, CO and H2O molecules as benchmark systems . 19 2.2.1 H2 ....................................... 19 ∗To whom correspondence should be addressed †Laboratoire Univers et Théories, Observatoire de Paris, 92190, Meudon, France ‡LOMC - UMR 6294, CNRS-Université du Havre, 25 rue Philippe Lebon, BP 540, 76058, Le Havre, France 1 2.2.2 CO . 22 2.2.3 H2O...................................... 27 2.3 Other recent results . 30 2.3.1 CN / HCN / HNC . 31 2.3.2 CS / SiO / SiS / SO / SO2 .......................... 34 2.3.3 NH3 /NH................................... 38 2.3.4 O2 / OH / NO . 40 2.3.5 C2 /C2H/C3 /C4 / HC3N.......................... 41 2.3.6 Complex Organic Molecules : H2CO / HCOOCH3 / CH3OH . 45 + + + + + 2.3.7 Cations : CH / SiH / HCO /N2H / HOCO . 49 + 2.3.8 H3 ...................................... 52 − − 2.3.9 Anions : CN /C2H ............................ 52 2.4 Isotopologues . 55 3 Radiative and chemical excitation 57 3.1 Radiative effects . 57 3.2 Chemical effects . 59 3.3 Examples .