Solid Oxygen Revisited Yu.A. Freiman H.J. Jodl Yanier Crespo 1
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Amarsinha D. Nikam Vital Force Is Oxygen Extrait Du Livre Vital Force Is Oxygen De Amarsinha D
Amarsinha D. Nikam Vital Force is Oxygen Extrait du livre Vital Force is Oxygen de Amarsinha D. Nikam Éditeur : B. Jain http://www.editions-narayana.fr/b9138 Sur notre librairie en ligne vous trouverez un grand choix de livres d'homéopathie en français, anglais et allemand. Reproduction des extraits strictement interdite. Narayana Verlag GmbH, Blumenplatz 2, D-79400 Kandern, Allemagne Tel. +33 9 7044 6488 Email [email protected] http://www.editions-narayana.fr Oxygen Oxygen is derived from the Greek word, where oxys means acid, literally sharp from the taste of acids and genes means producer, literally begetter. It is the element with atomic number 8 and represented by the symbol 'O'. It is a highly reactive non-metallic period 2 element that readily forms compounds (notably oxides) with almost all other elements. Oxygen is the third most abundant element in the universe by mass after hydrogen and helium. Diatomic oxygen gas constitutes 21% of the volume of air. Water is the most familiar oxygen compound. OXYGEN HISTORY Oxygen makes up 21% of the atmosphere we breathe, but it was not discovered as a separate gas until the late i8th century. Oxygen was independently discovered by Carl Wilhelm Scheele, in Uppsala in 1773 or earlier and by Joseph Priestley in Wiltshire, in 1774. The name oxygen was coined in 1777 by Antoine Lavoisier. Although oxygen plays a life-supporting role, it took Narayana Verlag, 79400 Kandern Tel.: 0049 7626 974 970 0 Excerpt from Dr. Amarsinha D.Nikam: Vital Force is Oxygen about 150 years for the gas to be used in a proper manner for patients. -
Chapter 16 Liquid and Solids
Homework #2 Chapter 16 Liquid and Solids 7. Vapor Pressure: The pressure exerted by the vapor of a liquid when the vapor and the liquid are in dynamic equilibrium. The vapor pressure reflects the fact that within a system there is a distribution of energies that molecules can have, therefore, some molecules will have enough energy to overcome the intermolecular forces and enter into the gas phase. All liquids have some vapor pressure. The stronger the intermolecular forces the smaller the vapor pressure. All solids also have a vapor pressure. This is why if you leave ice in the freezer for a long time it “disappears.” The vapor pressure of solids is less than the vapor pressure of liquids. As the temperature increases the molecules have more energy, therefore, more molecules can escape into the gas phase (vapor pressure increases). When the vapor pressure is equal to the atmospheric pressure the solution boils. 9. a) Surface Tension As the intermolecular forces increase (↑), surface tension increases (↑). b) Viscosity As the intermolecular forces increase (↑), the viscosity increases (↑). c) Melting Point As the intermolecular forces increase (↑), the melting point increases (↑). d) Boiling Point As the intermolecular forces increase (↑), the boiling point increases (↑). e) Vapor Pressure As the intermolecular forces increase (↑), the vapor pressure decreases (↓). 11. Intermolecular Forces: The forces of attraction/repulsion between molecules. Intramolecular Forces: The forces of attraction/repulsion within a molecule. Intramolecular forces are stronger the intermolecular forces. Types of intermolecular forces: Dipole-Dipole Forces: The interaction between two electric dipoles in different molecules. Hydrogen Bonding: The attraction between a hydrogen atom (that is bonded to an O, N, or F atom) and an O, N, or F atom in a neighboring molecule. -
The Properties of Oxygen Investigated with Easily Accessible Instrumentation the “One-Photon-Two-Molecule” Mechanism Revisited
In the Classroom The Properties of Oxygen Investigated with Easily Accessible Instrumentation The “One-Photon-Two-Molecule” Mechanism Revisited Manfred Adelhelm, Natasha Aristov, and Achim Habekost* Department of Chemistry, Padagogische Hochschule Ludwigsburg, Reuteallee 46, D-71634 Ludwigsburg, Germany *[email protected] Oxygen has spectacular and unusual properties (1). Students between the ground state and first excited state of oxygen, but are generally familiar with this gas as making up about 20% of the only if two ground-state molecules are promoted and relaxed to atmosphere, being required for combustion, participating in many two excited-state molecules. This has been nicely presented as an oxidation reactions, and being a colorless gas. The revelation that it exercise in spectral interpretation for the general chemistry is blue as a liquid and paramagnetic is surprising. The observation laboratory in this Journal (11). A key point to understanding that, under other conditions (as the product of a chemical the absorption spectrum was the observation of the same features reaction), oxygen emits red light, provides further amazement. both for gaseous oxygen at high pressures and for large oxygen- Over the years, several methods of demonstrating the paramag- layer thicknesses, on the order of the thickness of the earth's netic and optical properties of oxygen have been published in this atmosphere.1 Inter-molecular interactions, more likely in con- Journal (2-6). Using these demonstrations is an elegant way of densed or high-pressure phases and more likely to be seen in a gas introducing or reinforcing the concepts of molecular orbital (MO) reservoir as huge as the atmosphere, were proposed, and later theory. -
Agenda Jan 21, 2020 Return Notes Pages - a Couple of Things I Noticed
Agenda Jan 21, 2020 Return Notes pages - a couple of things I noticed Quick Check using your 13.3 notes Return notes - and I noticed a couple of areas I need to give you some additional insights. Kinetic Molecular Theory (for gases) The kinetic molecular theory is able to explain the behavior of most gases using the ideas that gas particles are very small, very far apart, moving quickly, colliding with each other and the walls of a container and that the higher the temperature the faster the particles are moving and the greater their average kinetic energy. In liquids the particles are still moving, but there are significant attractions in between molecules that hold them closer together in the flowing liquid phase. (intermolecular attractions) Intermolecular forces in liquids can result in properties like Viscosity - which is a measure of the resistance of a liquid to flow. It is determined by the type and strength of intermolecular forces in the liquid, the shape of the particles and temperature. As temperature increases the particles can flow more easily as they move more quickly, so the viscosity of the liquid decreases. Intermolecular forces in liquids can result in properties like Viscosity - which is a measure of the resistance of a liquid to flow. It is determined by the type and strength of intermolecular forces in the liquid, the shape of the particles and temperature. As temperature decreases the particles slow down and so the resistance to flow increases, in other words the viscosity increases. Intermolecular forces in liquids can result in properties like Surface tension and capillary action - which we will observe more closely after the Quick Check questions. -
LABORATORY STUDIES on the FORMATION of OZONE (O3) on ICY SATELLITES and on INTERSTELLAR and COMETARY ICES Chris J
The Astrophysical Journal, 635:1362–1369, 2005 December 20 # 2005. The American Astronomical Society. All rights reserved. Printed in U.S.A. LABORATORY STUDIES ON THE FORMATION OF OZONE (O3) ON ICY SATELLITES AND ON INTERSTELLAR AND COMETARY ICES Chris J. Bennett1 and Ralf I. Kaiser1,2,3 Received 2005 August 1; accepted 2005 August 25 ABSTRACT The formation of ozone (O3) in neat oxygen ices was investigated experimentally in a surface-scattering machine. At 11 K, solid oxygen was irradiated with energetic electrons; the chemical modification of the target was followed on-line and in situ via Fourier transform infrared spectroscopy (FTIR; solid state) and quadrupole mass spec- trometry (QMS; gas phase). The dominant product identified was the ozone molecule in the bent, C2v symmetric 1 structure, O3(X A1); the cyclic D3h isomer was not observed. The associated van der Waals complexes [O3 ...O] and [O3 ...O3] could also be detected via infrared spectroscopy, verifying explicitly the existence of oxygen atoms in the matrix at 11 K. Three different formation mechanisms of ozone were revealed. Two pathways involve the reaction 3 À of suprathermal oxygen atoms with molecular oxygen ½O2(X Æg ) at 11 K. Once the sample was warmed after the irradiation to about 38 K, a third, thermal reaction pathway involving the barrierless reaction of ground-state oxygen atoms with molecular oxygen sets in. During the warm-up phase, the inherent sublimation of oxygen and ozone was monitored by mass spectrometry and occurs in the ranges 28–43 and 58–73 K, respectively. Our data are of help to understand the mechanisms of ozone formation within apolar interstellar and cometary ices and could also be applicable to outer solar system icy bodies, such as the moons of Jupiter (Ganymede, Europa, and Callisto) and Saturn (Rhea and Dione), where ozone and/or condensed oxygen has been observed. -
13 Intermolecular Forces, Liquids, and Solids
13Intermolecular Forces, Liquids, and Solids The four types of solids Intermolecular Forces of Attraction • Ch 12 was all about gases… particles that don’t attract each other. Intermolecular Forces of Attraction • Ch 13 is about liquids and solids… where the attraction between particles allows the formation of solids and liquids. Intermolecular Forces of Attraction • These attractions are called “intermolcular forces of attractions” or IMF’s for short. • Intermolcular forces vs intramolecular forces Four Solids – Overview • Molecular Solids (particles with IMF’s) • Metals (metallic bonding) • Ionic Solids (ionic bonding) • Covalent Network Solids (covalent bonding) Molecular Solids • Molecules or noble gases (individual particles) Molecular Solid Examples • H O 2 • C2H5OH • CO2 • C6H12O6 • CH 4 • The alkanes, alkenes, etc. • NH 3 • The diatomic molecules • NO 2 • The noble gases • CO • C2H6 Metals • A lattice of positive ions in a “sea of electrons” • Metal atoms have low electronegativity Metal Examples • Pb • Brass (Cu + Zn) • Ag • Bronze (Cu + Sn) • Au • Stainless Steel (Fe/Cr/C) • Cu • Zn • Fe Ionic Solids • A lattice of positive and negative ions Ionic Solid Examples • NaCl • CaCl2 • KCl • MgSO4 • KI • Fe2O3 • FeCl3 • AgNO3 • CaCO3 • + ion & - ion Covalent Network Solids • Crystal held together with covalent bonds Covalent Network Solid Examples • C(diamond) • C(graphite) • SiO2 (quartz, sand, glass) • SiC • Si • WC • BN Properties of Metals Metals are good conductors of heat and electricity. They are shiny and lustrous. Metals can be pounded into thin sheets (malleable) and drawn into wires (ductile). Metals do not hold onto their valence electrons very well. They have low electronegativity. Properties of Ionic Solids • Brittle • High MP & BP • Dissolves in H2O • Conducts as (l), (aq), (g) Electrical Conductivity Intermolecular Forces (IMFs) • Each intermolecular force involves + and – attractions. -
Molecules to Materials 1
SERIES I ARTICLE Molecules to Materials 1. An Overview of Functional Molecular Solids T P Radhakrishnan With the advent of modern physics and chemistry, T P Radhakrishnan is in the School of Chemistry, fundamentally new types of materials have been created in Central University of this century. Various types of forces operating in different Hyderabad, classes of solids are exploited in the design of molecular Hyderabad 500 046. materials. A variety of fabrication techniques have been developed to make materials with the desired properties. An overview of these aspects is provided in this article. Historical Perspective The kinds of materials that have been developed and used over the course of history serve as excellent indicators of the evolution of technology, and civilisation at large. For instance, the early growth of civilisation has been described in terms of the stone, copper, bronze and iron ages. The earliest materials were those which were readily available in nature, like stone, clay and wood and the technology consisted' in reshaping and restructuring physically these materials to suit specific purposes such as weaponry and utensils. The most intricate process at this stage perhaps involved the fabrication of ceramics such as porcelain by baking clays, a practice that Discovery of dates back to the eighth millennium Be. Discovery of procedures for procedures for extraction of metals from their ores and extraction of fabrication of alloys was a major revolution in the history of metals from their materials. Here was a case of complete transformation of the ores and physical and chemical properties of a material. Equally fabrication of alloys fantastic was the discovery of glass-making, a process in was a major which the optical properties of the starting substance, sand, revolution in the are completely and drastically modified. -
Spiral Chain O4 Form of Dense Oxygen, Proc
This is a pre-print version of the following article: Li Zhu et al, Spiral chain O4 form of dense oxygen, Proc. Natl. Acad. Sci. U.S.A. (2011), doi: 10.1073/pnas.1119375109, which has been published online at http://www.pnas.org/content/early/2011/12/27/1119375109 Spiral Chain O4 Form of Dense Oxygen Li Zhua, Ziwei Wanga, Yanchao Wanga, Yanming Maa,*, Guangtian Zoua, and Ho-kwang Maob,* aState Key Laboratory of Superhard Materials, Jilin University, Changchun 130012, China; and bGeophysical Laboratory, Carnegie Institution of Washington, Washington, DC 20015 Oxygen is in many ways a unique element: the only known diatomic molecular magnet and the stabilization of the hitherto unexpected O8 cluster structure in its solid form at high pressure. Molecular dissociations upon compression as one of the fundamental problems were reported for other diatomic solids (e.g., H2, I2, Br2, and N2), but it remains elusive for molecular oxygen, making oxygen an intractable system. We here report the direct prediction on the dissociation of molecular oxygen into a polymeric spiral chain O4 structure (space group I41/acd, -O4) under terapascal (TPa) pressure by using first-principles method on crystal structure prediction. The -O4 stabilizes at above 1.92 TPa and has been earlier observed as the high pressure phase III of sulfur. We find that the molecular O8 phase remains extremely stable in a large pressure range of 0.008 – 1.92 TPa, whose breakdown is driven by the pressure-induced softening of a transverse acoustic phonon mode at the zone boundary V point, leading to the ultimate formation of -O4. -
Experiment Title: Solid Oxygen at High Temperature and High Pressure: a Study of a New Crystalline Phase Near the Melting Line
Experiment title: Solid Oxygen at High Temperature and Experiment High Pressure: a Study of a New Crystalline Phase near number: the Melting Line by Single-Crystal X-ray Diffraction HS2294 Beamline: Date of experiment: Date of report: from: November 22, 2004 to: November 25, 2004 Shifts: Local contact(s): Dr. Micheal Hanfland Received at ESRF: Names and affiliations of applicants (* indicates experimentalists): *S. Desgreniers, CEA/DAM Bruyères-le-Châtel, France and Département de physique, université d’Ottawa, Ottawa, Canada K1N 6N5 *G. Weck, CEA/DAM Bruyères-le-Châtel, France Report: Introduction The magnetic moment of the O2 molecule (S=1) and the resulting affinity to pairing, have been advanced to explain the rich phase diagram of solid oxygen under pressure and below 300 K in comparison to those of other solid molecular systems (e.g., H2, N2). Phases of solid oxygen at low temperature (T < 640K) and high pressures (P < 15 GPa) are well documented. In particular at 10 GPa and 300 K, solid oxygen transforms into a red-brown crystal with a monoclinic structure (space group: A2/m, Z=8): the ε-O2 phase. Recently, the nature of the magnetic interaction and ordering has been demonstrated from neutron diffraction experiments [1]. Furthermore, the nature of chemical changes induced by pressure, the density effect with the formation of O4 molecules [2] or collective effects with the formation of extended herringbone type chains [3], is still subject to discussion. At higher pressure, dense solid oxygen has been shown to undergo a semiconductor-to-metal transition [4] accompanied by a structural phase transition at 96 GPa [5, 6]. -
Structure, Energy, and Vibrational Frequencies of Oxygen Allotropes On
Article pubs.acs.org/JCTC Structure, Energy, and Vibrational Frequencies of Oxygen Allotropes On (n ≤ 6) in the Covalently Bound and van der Waals Forms: Ab Initio Study at the CCSD(T) Level † ‡ ⊥ § ∥ ⊥ † ∥ † Oleg B. Gadzhiev,*, , , Stanislav K. Ignatov,*, , , Mikhail Yu. Kulikov, , Alexander M. Feigin, § ‡ ∥ Alexey G. Razuvaev, Peter G. Sennikov, and Otto Schrems † Institute of Applied Physics, Russian Academy of Sciences, Nizhny Novgorod, 46 Ul’yanov Street, Nizhny Novgorod, 603950, Russia ‡ G.G. Devyatykh Institute of Chemistry of High Purity Substances, Russian Academy of Sciences, 49 Troponina St., Nizhny Novgorod, 603950, Russia § N.I. Lobachevsky State University of Nizhny Novgorod, National Research University, 23 Gagarin Avenue, Nizhny Novgorod, 603950, Russia ∥ Alfred Wegener Institute for Polar and Marine Research, Am Handelshafen 12, 27570 Bremerhaven, Germany *S Supporting Information ABSTRACT: Recent experiments on the UV and electron beam irradiation of solid O2 reveals a series of IR features near the valence antisymmetric vibration band of O3 which are frequently interpreted as the formation of unusual On allotropes in the forms of weak complexes or covalently bound molecules. In order to elucidate the question of the nature of the irradiation products, the structure, relative energies, and vibrational − frequencies of various forms of On (n =1 6) in the singlet, triplet, and, in some cases, quintet states were studied using the CCSD(T) method up to the CCSD(T,full)/cc-pCVTZ and CCSD(T,FC)/aug-cc-pVTZ levels. The results of calculations demonstrate the existence of stable highly symmetric structures O4 · · · ff (D3h), O4 (D2d), and O6 (D3d) as well as the intermolecular complexes O2 O2,O2 O3, and O3 O3 in di erent conformations. -
WATER CHEMISTRY CONTINUING EDUCATION PROFESSIONAL DEVELOPMENT COURSE 1St Edition
WATER CHEMISTRY CONTINUING EDUCATION PROFESSIONAL DEVELOPMENT COURSE 1st Edition 2 Water Chemistry 1st Edition 2015 © TLC Printing and Saving Instructions The best thing to do is to download this pdf document to your computer desktop and open it with Adobe Acrobat DC reader. Adobe Acrobat DC reader is a free computer software program and you can find it at Adobe Acrobat’s website. You can complete the course by viewing the course materials on your computer or you can print it out. Once you’ve paid for the course, we’ll give you permission to print this document. Printing Instructions: If you are going to print this document, this document is designed to be printed double-sided or duplexed but can be single-sided. This course booklet does not have the assignment. Please visit our website and download the assignment also. You can obtain a printed version from TLC for an additional $69.95 plus shipping charges. All downloads are electronically tracked and monitored for security purposes. 3 Water Chemistry 1st Edition 2015 © TLC We require the final exam to be proctored. Do not solely depend on TLC’s Approval list for it may be outdated. A second certificate of completion for a second State Agency $25 processing fee. Most of our students prefer to do the assignment in Word and e-mail or fax the assignment back to us. We also teach this course in a conventional hands-on class. Call us and schedule a class today. Responsibility This course contains EPA’s federal rule requirements. Please be aware that each state implements drinking water/wastewater/safety regulations may be more stringent than EPA’s or OSHA’s regulations. -
Chemistry 11 Ap – Bonding and Properties of Solids Worksheet
CHEMISTRY 11 AP – BONDING AND PROPERTIES OF SOLIDS WORKSHEET 1) Complete the following flowchart by filling in the boxes: Ionic/Covalent Metallic Ionic Network Covalent Covalent Molecular 2) Identify the type of solid shown by each of the following diagrams. Explain the types of particles and bonding represented by the diagram. (a) (c) Ionic solid since the particles are positive and Covalent molecular solid since the particles are negative ions that are held together by molecules that are held together by weak electrostatic attraction between oppositely intermolecular forces. charged particles. (b) (d) Network covalent solid since the particles are Metallic solids since the particles are positive atoms which are covalently bonded to each other ions and delocalized electrons. The metal is held forming an extremely large lattice structure. together by the attraction between the positive ions and the negative delocalized electrons. 3) Classify Ge, RbI, C6(CH3)6 and Zn according to their type of solid and arrange them in order of increasing melting point. Explain. Germanium is located on the periodic table just under silicon, along the diagonal line of metalloids, which suggests that elemental Ge is likely to have the same structure as Si (a tetrahedral diamond structure). Therefore Ge is probably a network covalent solid and would have an incredibly high melting point. RbI is an ionic solid and would have a high melting point. C6(CH3)6 is a combination of non-metals forming a covalent molecular solid which will form isolated molecules with weak intermolecular forces between them. Therefore C6(CH3)6 will have a low melting point due to the ease with which these weak IMFs can be broken.