Lectures 1-2: Introduction to Atomic Spectroscopy Types of Spectra
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Glossary Physics (I-Introduction)
1 Glossary Physics (I-introduction) - Efficiency: The percent of the work put into a machine that is converted into useful work output; = work done / energy used [-]. = eta In machines: The work output of any machine cannot exceed the work input (<=100%); in an ideal machine, where no energy is transformed into heat: work(input) = work(output), =100%. Energy: The property of a system that enables it to do work. Conservation o. E.: Energy cannot be created or destroyed; it may be transformed from one form into another, but the total amount of energy never changes. Equilibrium: The state of an object when not acted upon by a net force or net torque; an object in equilibrium may be at rest or moving at uniform velocity - not accelerating. Mechanical E.: The state of an object or system of objects for which any impressed forces cancels to zero and no acceleration occurs. Dynamic E.: Object is moving without experiencing acceleration. Static E.: Object is at rest.F Force: The influence that can cause an object to be accelerated or retarded; is always in the direction of the net force, hence a vector quantity; the four elementary forces are: Electromagnetic F.: Is an attraction or repulsion G, gravit. const.6.672E-11[Nm2/kg2] between electric charges: d, distance [m] 2 2 2 2 F = 1/(40) (q1q2/d ) [(CC/m )(Nm /C )] = [N] m,M, mass [kg] Gravitational F.: Is a mutual attraction between all masses: q, charge [As] [C] 2 2 2 2 F = GmM/d [Nm /kg kg 1/m ] = [N] 0, dielectric constant Strong F.: (nuclear force) Acts within the nuclei of atoms: 8.854E-12 [C2/Nm2] [F/m] 2 2 2 2 2 F = 1/(40) (e /d ) [(CC/m )(Nm /C )] = [N] , 3.14 [-] Weak F.: Manifests itself in special reactions among elementary e, 1.60210 E-19 [As] [C] particles, such as the reaction that occur in radioactive decay. -
Or Continuous Spectrum and Not to the Line Spectra. in the X-Ray Region, In
662 PHYSICS: W. D UA NE PROC. N. A. S. intensity is greatest close to -80 and that it falls off regularly as the angle departs therefrom. We conclude, therefore, that the momentum of the electron in its orbit uithin the atom does not affect the direction of ejection in the way denanded by the theory of Auger and Perrin. While this does not constitute definite evidence against the physical reality of electronic orbits, it is a serious difficulty for the conception. A detailed discussion of the general question here raised in the light of new experimental results will be published elsewhere. 1 Auger, P., J. Physique Rad., 8, 1927 (85-92). 2 Loughridge, D. H., in press. 3 Bothe, W., Zs. Physik, 26, 1924 (59-73). 4 Auger, P., and Perrin, F., J. Physique Rad., 8, 1927 (93-111). 6 Bothe, W., Zs. Physik, 26,1924 (74-84). 6 Watson, E. C., in press. THE CHARACTER OF THE GENERAL, OR CONTINUOUS SPEC- TRUM RADIA TION By WILLIAM DuANX, DJPARTMSNT OF PHysIcs, HARVARD UNIVERSITY Communicated August 6, 1927 The impacts of electrons against atoms produce two different kinds of radiation-the general, or continuous spectrum and the line spectra. By far the greatest amount of energy radiated belongs to the general, or continuous spectrum and not to the line spectra. In the X-ray region, in particular, the continuous, or general radiation spectrum carries most of the radiated energy. In spite of this, and because the line spectra have an important bearing on atomic structure, the general radiation has received much less attention than the line spectra in the recent de- velopment of fundamental ideas in physical science. -
Discrete-Continuous and Classical-Quantum
Under consideration for publication in Math. Struct. in Comp. Science Discrete-continuous and classical-quantum T. Paul C.N.R.S., D.M.A., Ecole Normale Sup´erieure Received 21 November 2006 Abstract A discussion concerning the opposition between discretness and continuum in quantum mechanics is presented. In particular this duality is shown to be present not only in the early days of the theory, but remains actual, featuring different aspects of discretization. In particular discreteness of quantum mechanics is a key-stone for quantum information and quantum computation. A conclusion involving a concept of completeness linking dis- creteness and continuum is proposed. 1. Discrete-continuous in the old quantum theory Discretness is obviously a fundamental aspect of Quantum Mechanics. When you send white light, that is a continuous spectrum of colors, on a mono-atomic gas, you get back precise line spectra and only Quantum Mechanics can explain this phenomenon. In fact the birth of quantum physics involves more discretization than discretness : in the famous Max Planck’s paper of 1900, and even more explicitly in the 1905 paper by Einstein about the photo-electric effect, what is really done is what a computer does: an integral is replaced by a discrete sum. And the discretization length is given by the Planck’s constant. This idea will be later on applied by Niels Bohr during the years 1910’s to the atomic model. Already one has to notice that during that time another form of discretization had appeared : the atomic model. It is astonishing to notice how long it took to accept the atomic hypothesis (Perrin 1905). -
Atomic and Molecular Laser-Induced Breakdown Spectroscopy of Selected Pharmaceuticals
Article Atomic and Molecular Laser-Induced Breakdown Spectroscopy of Selected Pharmaceuticals Pravin Kumar Tiwari 1,2, Nilesh Kumar Rai 3, Rohit Kumar 3, Christian G. Parigger 4 and Awadhesh Kumar Rai 2,* 1 Institute for Plasma Research, Gandhinagar, Gujarat-382428, India 2 Laser Spectroscopy Research Laboratory, Department of Physics, University of Allahabad, Prayagraj-211002, India 3 CMP Degree College, Department of Physics, University of Allahabad, Pragyagraj-211002, India 4 Physics and Astronomy Department, University of Tennessee, University of Tennessee Space Institute, Center for Laser Applications, 411 B.H. Goethert Parkway, Tullahoma, TN 37388-9700, USA * Correspondence: [email protected]; Tel.: +91-532-2460993 Received: 10 June 2019; Accepted: 10 July 2019; Published: 19 July 2019 Abstract: Laser-induced breakdown spectroscopy (LIBS) of pharmaceutical drugs that contain paracetamol was investigated in air and argon atmospheres. The characteristic neutral and ionic spectral lines of various elements and molecular signatures of CN violet and C2 Swan band systems were observed. The relative hardness of all drug samples was measured as well. Principal component analysis, a multivariate method, was applied in the data analysis for demarcation purposes of the drug samples. The CN violet and C2 Swan spectral radiances were investigated for evaluation of a possible correlation of the chemical and molecular structures of the pharmaceuticals. Complementary Raman and Fourier-transform-infrared spectroscopies were used to record the molecular spectra of the drug samples. The application of the above techniques for drug screening are important for the identification and mitigation of drugs that contain additives that may cause adverse side-effects. Keywords: paracetamol; laser-induced breakdown spectroscopy; cyanide; carbon swan bands; principal component analysis; Raman spectroscopy; Fourier-transform-infrared spectroscopy 1. -
Absorption Spectroscopy and Imaging from the Visible Through Mid-Infrared with 20 Nm Resolution
Absorption spectroscopy and imaging from the visible through mid-infrared with 20 nm resolution. Aaron M. Katzenmeyer,1 Glenn Holland,1 Kevin Kjoller2 and Andrea Centrone1* 1Center for Nanoscale Science and Technology, National Institute of Standards and Technology, 100 Bureau Drive, Gaithersburg, Maryland 20899, United States. *E-mail: [email protected] 2Anasys Instruments, Inc., 325 Chapala Street, Santa Barbara, California 93101, United States. Abstract Absorption spectroscopy and mapping from visible through mid-IR wavelengths has been achieved with spatial resolution exceeding the limit imposed by diffraction, via the photothermal induced resonance technique. Correlated vibrational (chemical), and electronic properties are obtained simultaneously with topography with a wavelength-independent resolution of ≈ 20 nm using a single laboratory-scale instrument. This marks the highest resolution reported for PTIR, as determined by comparing height and PTIR images, and its first extension to near-IR and visible wavelengths. Light-matter interaction enables scientists to characterize materials and biological samples across a large range of energies. Visible (VIS) and near-infrared (NIR) light (from 400 nm to 2.5 µm) probes electronic transitions in materials [1], providing information regarding band gap, defects, and energy transfer which is crucial for the semiconductor and optoelectronic industries and for understanding processes such as photosynthesis. Mid-infrared (mid-IR) light (from 2.5 µm to 15 µm) probes vibrational transitions and provides rich chemical and structural information enabling materials identification [2]. Spectral maps can be obtained by coupling a light source and a spectrometer with an optical microscope [3]. However, light diffraction limits the lateral resolution achievable with conventional microscopic techniques to approximately half the wavelength of light [4]. -
Absorption Spectroscopy
World Bank & Government of The Netherlands funded Training module # WQ - 34 Absorption Spectroscopy New Delhi, February 2000 CSMRS Building, 4th Floor, Olof Palme Marg, Hauz Khas, DHV Consultants BV & DELFT HYDRAULICS New Delhi – 11 00 16 India Tel: 68 61 681 / 84 Fax: (+ 91 11) 68 61 685 with E-Mail: [email protected] HALCROW, TAHAL, CES, ORG & JPS Table of contents Page 1 Module context 2 2 Module profile 3 3 Session plan 4 4 Overhead/flipchart master 5 5 Evaluation sheets 22 6 Handout 24 7 Additional handout 29 8 Main text 31 Hydrology Project Training Module File: “ 34 Absorption Spectroscopy.doc” Version 06/11/02 Page 1 1. Module context This module introduces the principles of absorption spectroscopy and its applications in chemical analyses. Other related modules are listed below. While designing a training course, the relationship between this module and the others, would be maintained by keeping them close together in the syllabus and place them in a logical sequence. The actual selection of the topics and the depth of training would, of course, depend on the training needs of the participants, i.e. their knowledge level and skills performance upon the start of the course. No. Module title Code Objectives 1. Basic chemistry concepts WQ - 02 • Convert units from one to another • Discuss the basic concepts of quantitative chemistry • Report analytical results with the correct number of significant digits. 2. Basic aquatic chemistry WQ - 24 • Understand equilibrium chemistry and concepts ionisation constants. • Understand basis of pH and buffers • Calculate different types of alkalinity. -
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. -
Atomic Spectroscopy
Atomic Spectroscopy Reference Books: 1) Analytical Chemistry by Gary D. Christian 2) Principles of instrumental Analysis by Skoog, Holler, Crouch 3) Fundamentals of Analytical Chemistry by Skoog 4) Basic Concepts of analytical Chemistry by S. M. Khopkar We consider two types of optical atomic spectrometric methods that use similar techniques for sample introduction and atomization. The first is atomic absorption spectrometry (AAS), which for half a century has been the most widely used method for the determination of single elements in analytical samples. The second is atomic fluorescence spectrometry (AFS), which since the mid-1960s has been studied extensively. By contrast to the absorption method, atomic fluorescence has not gained widespread general use for routine elemental analysis. Thus, although several instrument makers have in recent years begun to offer special- purpose atomic fluorescence spectrometers, the vast majority of instruments are still of the atomic absorption type. Sample Atomization Techniques We first describe the two most common methods of sample atomization encountered in AAS and AFS, flame atomization, and electrothermal atomization. We then turn to three specialized atomization procedures used in both types of spectrometry. Flame Atomization In a flame atomizer, a solution of the sample is nebulized by a flow of gaseous oxidant, mixed with a gaseous fuel, and carried into a flame where atomization occurs. As shown in Figure, a complex set of interconnected processes then occur in the flame. The first step is desolvation, in which the solvent evaporates to produce a finely divided solid molecular aerosol. The aerosol is then volatilized to form gaseous molecules. Dissociation of most of these molecules produces an atomic gas. -
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. -
Methods Employed in Optical Emission Spectroscopy Analysis: a Review
Ingeniería y Ciencia ISSN:1794-9165 | ISSN-e: 2256-4314 ing. cienc., vol. 11, no. 21, pp. 239–267, enero-junio. 2015. http://www.eafit.edu.co/ingciencia This article is licensed under a Creative Commons Attribution 4.0 By Methods Employed in Optical Emission Spectroscopy Analysis: a Review D. M. Devia 1, L. V. Rodriguez-Restrepo 2and E. Restrepo-Parra 3 Received: 15-06-2014 | Acepted: 25-09-2014 | Onlínea: 01-30-2015 PACS: 52.25.Dg, 31.15.V- doi:10.17230/ingciencia.11.21.12 Abstract In this work, different methods employed for the analysis of emission spec- tra are presented. The proposal is to calculate the excitation temperature (Texc), electronic temperature (Te) and electron density (ne) for several plasma techniques used in the growth of thin films. Some of these tech- niques include magnetron sputtering and arc discharges. Initially, some fundamental physical principles that support the Optical Emission Spec- troscopy (OES) technique are described; then, some rules to consider dur- ing the spectral analysis to avoid ambiguities are listed. Finally, some of the more frequently used spectroscopic methods for determining the phy- sical properties of plasma are described. Key words: OES; plasma parameters; elemental determination; line intensity; broadening; shifting 1 Universidad Tecnológica de Pereira, Pereira, Colombia, [email protected]. 2 Universidad Nacional de Colombia, Sede Manizales, Colombia, [email protected] . 3 Universidad Nacional de Colombia, Sede Manizales, Colombia [email protected]. Universidad EAFIT 239j Methods Employed in Optical Emission Spectroscopy Analysis: a Review Métodos empleados en el análisis de espectroscopía óptica de emisión: una revisión Resumen En este trabajo se presentan diferentes métodos empleados para el análisis de espectros ópticos de emisión.