Academic literature on the topic 'MUONIUM'

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Journal articles on the topic "MUONIUM"

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Stadlbauer, John M., Krishnan Venkateswaran, Hugh A. Gillis, Gerald B. Porter, and David C. Walker. "Micelle-induced change of mechanism in the reaction of muonium with acetone." Canadian Journal of Chemistry 74, no. 11 (November 1, 1996): 1945–51. http://dx.doi.org/10.1139/v96-221.

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Muonium atoms add to the O atom of the carbonyl group of acetone to give the muonated free radical (CH3)2Ċ-O-Mu when the reaction takes place in water or hydrocarbons, but not when the acetone is localized in micelles. Micelles have no effect on the formation of muonated cyclohexadienyl radicals when muonium reacts with benzene under similar conditions. The addition reaction with acetone appears to have been subsumed by a faster alternative reaction in the micellar environment. Evidence is presented for this interpretation rather than for an inhibition of the radical or for a shift in the muon level-crossing resonance spectrum with hydrogen (muonium) bonding, though major shifts are seen for the spectrum of this radical in pure solvents of widely different dielectric constant. It is suggested that muonium's "abstraction" reaction takes over in micelles because significant micelle-induced enhancement effects were previously observed in that type of reaction. The data are consistent with a rate constant for the abstraction reaction of muonium with acetone in micelles of >6 × 108 M−1 s−1. Key words: muonium, kinetic isotope effects, micelle enhancement, H/Mu-addition, H/Mu abstraction.
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2

Lamm, Henry, and Yao Ji. "Predicting and Discovering True Muonium (μ+μ−)." EPJ Web of Conferences 181 (2018): 01016. http://dx.doi.org/10.1051/epjconf/201818101016.

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The recent observation of discrepancies in the muonic sector motivates searches for the yet undiscovered atom true muonium (μ+μ−). To leverage potential experimental signals, precise theoretical calculations are required. I will present the on-going work to compute higher-order corrections to the hyperfine splitting and the Lamb shift. Further, possible detection in rare meson decay experiments like REDTOP and using true muonium production to constrain mesonic form factors will be discussed.
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Koppenol, W. H. "Names for muonium and hydrogen atoms and their ions(IUPAC Recommendations 2001)." Pure and Applied Chemistry 73, no. 2 (January 1, 2001): 377–79. http://dx.doi.org/10.1351/pac200173020377.

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Muons are short-lived species with an elementary positive or negative charge and a mass 207 times that of the electron. These recommendations concern positive muons, given the short lifetime of negative muons. A positive muon mimics a light hydrogen nucleus, and names are given in analogy to existing names for hydrogen-containing compounds. A particle consisting of a positive muon and an electron (µ+ e -) is named "muonium" and has the symbol Mu. Examples: "muonium chloride," MuCl, is the equivalent of deuterium chloride, 2 HCl or DCl; "muoniomethane", CH 3 Mu, is the product of the muoniation of methane;and NaMu is "sodium muonide."
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Putlitz, G. zu. "Muonium." Hyperfine Interactions 103, no. 1 (December 1996): 157–70. http://dx.doi.org/10.1007/bf02317351.

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Hughes, Vernon W. "Muonium." Zeitschrift für Physik C Particles and Fields 56, S1 (March 1992): S35—S43. http://dx.doi.org/10.1007/bf02426773.

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Boikova, Natalya Adamovna, Olga Alexeevna Boikova, and Yuri’ Nikolatvitch Tyuhtyaev. "Electromagnetic Interaction for Muonium and Muonic Hydrogen." Izvestiya of Saratov University. New series. Series: Physics 11, no. 1 (2011): 52–58. http://dx.doi.org/10.18500/1817-3020-2011-11-1-52-58.

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Kulhar, V. S. "Muonium/muonic hydrogen formation in atomic hydrogen." Pramana 63, no. 3 (September 2004): 543–51. http://dx.doi.org/10.1007/bf02704482.

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Walker, David C. "Isotope effects in solution: contrasts between muonium and hydrogen in reactions with acetone." Canadian Journal of Chemistry 68, no. 10 (October 1, 1990): 1719–24. http://dx.doi.org/10.1139/v90-267.

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Munonium atoms are hydrogen isotopes with positive muons rather than protons, deuterons, or tritons as nuclei. Thus, they have one ninth the mass of 1H, and microsecond lifetimes. By using nuclear physics counting techniques, muonium can be studied in a wide variety of media and its chemical and physical properties used to appraise hydrogen. Results are described for the interaction of muonium with acetone, showing two types of kinetic isotope effects, formation of free radicals, evidence for intermolecular "muonium bonding", and micelle-induced enhancements of reaction rate constants. Keywords: isotope effects, muonium atoms, muonium bonding, thiyl radicals, micelles.
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Walker, David C., Stefan Karolczak, Hugh A. Gillis, and Gerald B. Porter. "Hot model of muonium formation in liquids." Canadian Journal of Chemistry 81, no. 3 (March 1, 2003): 199–203. http://dx.doi.org/10.1139/v03-011.

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The mechanism of formation of muonium atoms from positive muons was studied here through measurements of the yield of diamagnetic muon states in dipolar aprotic solvents and for scavenger solutions in hexane and methanol. The results are compared with published data on common solvents covering a full range of the physicochemical properties of liquids that affect an ionic formation mechanism, namely their static dielectric constants, electron mobilities, and radiolysis yields of electrons. It is concluded that muonium is not formed by a thermal charge-neutralization reaction in these chemically-active media, though that mechanism does contribute to muonium formation in inert media like liquefied noble gases. It is clear that muonium materializes on a much shorter timescale than the recently proposed "delayed" mechanism (microseconds) and the earlier "spur" model (nanoseconds). In contrast, the data referring to all these liquids are consistent with the intra-track "hot" model. This is the only Mu-formation model proposed so far in which the immediate precursors of Mu (Mu(hot)) are neither scavengable nor ionic.Key words: muonium atoms, formation mechanism, hot model, spur model, delayed-muonium-formation model, diamagnetic yields.
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Karolczak, Stefan, Hugh A. Gillis, Gerald B. Porter, and David C. Walker. "Solvent-dependent rate constants of muonium atom reactions." Canadian Journal of Chemistry 81, no. 2 (February 1, 2003): 175–78. http://dx.doi.org/10.1139/v03-009.

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The rates of reaction of muonium atoms with solutes, ionic and organic, were studied in solvents of wildly differing polarities (water, methanol, and hexane) and their rate constants were compared, where possible. In these reactions — which are those of a highly reactive atom, an isotope of hydrogen — it transpires that the reaction rates are higher in solvents in which the solute is more soluble and muonium diffuses faster. This study leads to various kinetic-solvent-effect ratios and to the observation of the reaction of muonium with free radicals being among the fastest reactions recorded so far between two neutral species in solution.Key words: muonium atoms, kinetic isotope effects, solvent-dependent rates, non-aqueous solvents, muon spin rotation technique.
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Dissertations / Theses on the topic "MUONIUM"

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Fry, Charles Alan. "Measurement of the Lamb shift in muonium." Thesis, University of British Columbia, 1985. http://hdl.handle.net/2429/25785.

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This thesis describes the first measurement of the Lamb shift in n=2 muonium. The muonium atom is a hydrogen-like bound state of two leptons (µ⁺e⁻), both of which are believed to be point-like particles. The point-like nature of the constituent particles simplifies and reduces the uncertainty of the application of quantum electrodynamics (QED) to the calculation of the Lamb shift in the muonium atom. Measurements of the Lamb shift in hydrogen disagree with the predictions of theory by a few standard deviations; however, theoretical predictions also disagree with each other, partly because of difficulties associated with the treatment of the proton structure. Thus a measurement in the muonium system of similar precision to those already made in the hydrogen system will be a valuable test of QED. The present experiment is not intended to test QED. It is an investigation of the methods and techniques necessary to surmount the difficulties presented by the nature of muonium. The available number of muonium atoms is about 10⁺¹º times less than that of hydrogen used by Lamb in his first measurement. The value obtained for the n=2 muonium Lamb shift 1070⁺¹²₋₁₅ MHz. The uncertainty quoted is statistical at the 68% confidence level. Systematic effects were found to contribute to a further 2 MHz uncertainty.
Science, Faculty of
Physics and Astronomy, Department of
Graduate
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Spencer, David Philip. "Muonium in some insulating oxides and diamond." Thesis, University of British Columbia, 1985. http://hdl.handle.net/2429/25972.

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Muonium can be regarded as an isotopic analogue of the hydrogen atom, with a positive muon replacing the proton. This thesis is concerned with searches for muonium in weak transverse and zero magnetic fields in a variety of non-magnetic oxide insulators with few nuclear moments, and in diamond, a semiconductor. The technique of Muon Spin Rotation (µSR) was used, which can be thought of in analogy with NMR and EPR. It relies on measuring the direction of the muon spin with time via the unique signature of the parity violating decay of the muon, in which its decay positron is emitted preferentially along the muon spin direction. This can provide a sensitive measure of the interaction of the muon spin with its environment. Muonium has been searched for successfully in ɑ-quartz, fused quartz., hexagonal and fused germanium dioxide, magnesium oxide, and diamond; and unsuccessfully in tetragonal germanium dioxide, rutile, strontium titanate, zircon, and beryl. All the samples save the quartzes showed a large "missing fraction"; that is, not all the initial muon polarization could be accounted for. This indicates that muonium was formed but rapidly depolarized. The missing fractions were found to be very strongly temperature dependent in strontium titanate but only weakly in rutile. At room temperature, the observed muonium fractions were: ɑ-quartz and fused quartz (65±5)%, hexagonal germanium dioxide <2%, fused germanium dioxide (10±4)%, magnesium oxide (30±10)%, and diamond (33± 4)%. It is noteworthy that the fractions are very different in quartz and germanium dioxide, despite their structural analogy. The observation of muonium in diamond represents the first time that muonium has been seen in a room temperature semiconductor. A spin-Hamiltonian new to µSR was found in low-temperature ɑ-quartz and hexagonal germanium dioxide, in which the hyperfine interaction is completely anisotropic. In low-temperature ɑ-quartz in zero magnetic field this interaction gives rise to three signals whose frequencies are orientation independent, but whose amplitudes are strongly orientation dependent By studying the orientation dependence it was determined that muonium occupies a site which is identical with that seen for hydrogen in EPR studies. This was the first time that muonium was shown to behave just like an isotope of hydrogen in a solid. In hexagonal GeO₂, eight frequencies were observed at 6K, in marked contrast to the observation of only three frequencies in structurally analogous ɑ-quartz. The interpretation of this is that there are three or four different sites, the exact nature of which has not been determined.
Science, Faculty of
Chemistry, Department of
Graduate
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Morris, Gerald D. "Muonium formation and diffusion in cryocrystals." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/nq27205.pdf.

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Barnabas, Mary Vijayarani. "Reactions of muonium and positronium in solution." Thesis, University of British Columbia, 1989. http://hdl.handle.net/2429/29007.

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Positive muons are produced at TRIUMF as pion decay products and form muo-nium atoms in media such as water during their two microsecond lifetime. Muo-nium is a hydrogen-like atom with virtually the same Bohr radius and ionization energy as ¹H, ²H and ³H, but with a mass one-ninth that of ¹H. Its reactions toward solutes are studied by μSR (the muon spin rotation technique) and the muonated free radicals it forms are studied by μLCR (muon level crossing resonance spectroscopy). In this thesis, rate constants for muonium reactions were determined for a range of solutes from simple amides to DNA bases. Their values ranged from <10⁵ M⁻¹s⁻¹ to >10¹⁰M⁻¹s⁻¹. Kinetic isotope effects (relative to-¹H) varied from 100 to 0.01 depending on the reaction-type. In the presence of added micelles the rates of some abstraction reactions were very greatly enhanced, whereas most addition reactions were unaffected by the micellar microenvironment. Muonium was seen by LCR spectroscopy to add at a diffusion-limited rate across thiocarbonyl groups, with muonium attached to the carbon and thus yielding thiyl radicals. Uracil and thymine were studied by both μSR and LCR and their relative addition probabilities at C(5) and C(6) were determined. Ortho-positronium (the atom consisting of an electron-positron pair with parallel spins) was studied by the positron annihilation lifetime technique for comparison with muonium in most of these same solutions. Its reactions are different, not 'adding' or 'abstracting' for instance, and it shows none of the properties of a hydrogen isotope.
Science, Faculty of
Chemistry, Department of
Graduate
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Harshman, Dale Richard. "The interactions of muonium with silica surfaces." Thesis, University of British Columbia, 1986. http://hdl.handle.net/2429/27108.

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The behavior of muonium on the surface of fine (35 Å mean radius) SiO₂ powders has been studied using the techniques of muon spin rotation (μSR). Results indicate diffusion and trapping behavior of the muonium atoms on the silica surface, which is strongly influenced by the concentration of surface hydroxyl groups. Specifically, the presence of the surface hydroxyl groups has been shown to inhibit the motion of muonium on the silica surface. These studies have also provided information regarding the origin of the relaxation of the muon spin polarization for muonium on the silica surface. Specifically, a random anisotropic distortion of the muonium hyperfine interaction, induced by the local surface environment of the muonium atom, has been shown to be a principal contributor to the relaxation of the muon ensemble spin polarization, whereas the random local magnetic fields due to the neighboring hydroxyl protons were found to play only a minor role. From this result, the observed strong dependence of the relaxation on the surface hydroxyl concentration has been attributed to an associated hyperfine distortion, induced by the neighboring hydroxyls. A new spin relaxation theory, for the case of random anisotropic hyperfine distortions, has also been developed to explain the data. Gas adsorption isotherm studies were also performed, with ⁴He at 6 K, which show the muonium asymmetry to be strongly influenced by the fractional surface coverage. These results clearly indicate that the muonium formation probability decreases with increasing surface coverage, suggesting that the charge exchange cross section at the silica surface is significant. The implication of these results with regard to the origins of muonium formation (i.e., surface or bulk formation) is as yet unclear, however, since the precise role played by the adsorbed helium atoms is not known. These investigations have also been extended to platinum loaded silica, where the first surface reaction of muonium has been observed; the reaction rate of muonium with the surface of oxygen-covered platinum microcrystals was found to be 3.5 ± 0.15 μs⁻¹.
Science, Faculty of
Physics and Astronomy, Department of
Graduate
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Tempelmann, Alexandra. "Reaction kinetics of muonium with hydrogen bromide." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/30385.

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The rate constants of the abstraction reaction Mu + HBr —• MuH + Br were measured using the well established μSR technique at TRIUMF. Measurements were made at various temperatures between 170 and 480 K, and fit to the Arrhenius equation both with and without an additional T½ dependence. The rate constants obtained were k(T) = (5.101 ± 0.106) x 10⁻¹¹ exp{-(0.560 ± 0.110) kcal mol⁻¹/RT} and k(T) = (0.183 ± 0.005) x 10⁻¹¹T½exp{-(0.286± 0.014) kcal mol⁻¹/RT} cm³ molecule⁻¹ s⁻¹. The low activation energy for such an exothermic reaction indicates that the barrier on the Mu + HBr surface is early. Kinetic isotope effects of the H/Mu + HBr reactions along with a lack of curvature in the Mu + HBr Arrhenius plot suggest that tunneling is relatively unimportant down to 170 K.
Science, Faculty of
Chemistry, Department of
Graduate
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7

Yen, Hon Kit. "Theoretical spin dynamics on muonium level-crossing resonance." Thesis, University of British Columbia, 1988. http://hdl.handle.net/2429/28531.

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Redfield's theory and the theory of master equations have been reviewed and their applications to muonium spin dynamics discussed. It was found that both theories are equivalent in the Markov limit. In some cases, analytical expressions for relaxation rates are found. In addition, Redfield's theory was applied to describe spin relaxation of muonium-substituted free radicals near level-crossing resonances. Theoretical predictions were compared with experimental data for the C₆F₆-Mu radical and the results suggest there are several relaxation mechanisms involved.
Science, Faculty of
Physics and Astronomy, Department of
Graduate
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8

Hubbard, Penny Louise. "Molecular and electron dynamics with muon spectroscopy." Thesis, University of East Anglia, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.268573.

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Bakule, Pavel. "A solid state laser system for Doppler-free spectroscopy of muonium." Thesis, University of Oxford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.365885.

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Kerridge, Andrew. "Quantum behaviour of hydrogen and muonium in solid-state and biological systems." Thesis, University College London (University of London), 2004. http://discovery.ucl.ac.uk/1446780/.

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For hydrogen-like nuclei (HLN) such as the proton or muon, the quantum zero point energy cannot be ignored. The main objectives of this thesis were to identify practical ways to model this quantatively, and hence i) to gain an understanding of interactions between the HLN and its environment, and ii) to use this understanding to evaluate the wavefunction of such a nucleus within an electronic structure calculation. Several features of the HLN-electron interactions were studied analytically by assuming their interaction to be harmonic in nature. It was shown that the accurate modelling of the HLN-electron correlation was extremely important in the evaluation of the HLN wavefunction. A parametrised correlation model (PCM) was developed, and was shown to accurately reproduce the effective potential energy surface experienced by the HLN when HLN-electron correlation was included. The required parameters showed a simple HLN mass dependence. The PCM was used to study DNA base molecule adducts formed by addition of a single HLN. The relative stability of these adducts was shown to be dependent on the mass of the HLN, and the inclusion of HLN-electron correlation was shown to lead to a stabilisation of the C-X bonds relative to the N-X and O-X bonds. The PCM was used to study the interaction of H and Mu with the diamond dopants sulphur and phosphorus. The PCM correctly predicted differences between the HLN wavefunctions in crystalline and molecular environments. The HLN-electron correlation energy was shown to be large enough to cause the phosphorus-muonium defect complex formation energy to become positive. HLN-impurity-vacancy complexes in diamond were studied using the PCM, and it was found that the lowest energy state was obtained by the HLN saturating a carbon dangling bond, irrespective of the impurity species. It was concluded that the HLN would be effectively localised at a single site.
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Books on the topic "MUONIUM"

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service), SpringerLink (Online, ed. Muonium-antimuonium Oscillations in an Extended Minimal Supersymmetric Standard Model. New York, NY: Springer Science+Business Media, LLC, 2011.

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Liu, Boyang. Muonium-antimuonium Oscillations in an Extended Minimal Supersymmetric Standard Model. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-8330-5.

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In memory of Vernon Willard Hughes: Proceedings of the Memorial Symposium in Honor of Vernon Willard Hughes, Yale University, USA, 14-15 Novmber 2003. Singapore: World Scientific, 2005.

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University), Vernon Willard Hughes Memorial Symposium (2003 Yale. In memory of Vernon Willard Hughes: Proceedings of the Memorial Symposium in Honor of Vernon Willard Hughes, Yale University, USA, 14-15 Novmber 2003. Hackensack, NJ: World Scientific, 2004.

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Schaller, Lukas A., and Claude Petitjean, eds. Muonic Atoms and Molecules. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-7271-3.

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Rigby, David Alan. Measurement of the muonic branching ratio of the [tau] lepton using the OPAL detector at LEP. Birmingham: University of Birmingham, 1996.

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Liu, Boyang. Muonium-antimuonium Oscillations in an Extended Minimal Supersymmetric Standard Model. Springer, 2014.

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Liu, Boyang. Muonium-antimuonium Oscillations in an Extended Minimal Supersymmetric Standard Model. Springer, 2011.

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(Editor), Emlyn Willard Hughes, and Francesco Iachello (Editor), eds. In Memory Of Vernon Willard Hughes: Proceedings Of The Memorial Symposium In Honor Of Vernon Willard Hughes, Yale University, USA 14 - 15 November 2003. World Scientific Publishing Company, 2004.

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1936-, Davis E. A., and Cox S. F. J, eds. Protons and muons in materials science. London: Taylor & Francis, 1996.

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Book chapters on the topic "MUONIUM"

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Hughes, Vernon W. "Muonium." In The Future of Muon Physics, 35–43. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-77960-2_8.

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Hughes, Vernon W. "Muonium." In Fundamental Symmetries, 287–300. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-5389-8_25.

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Jungmann, Klaus P. "Muonium Spectroscopy." In Muonic Atoms and Molecules, 77–82. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-7271-3_7.

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Cox, S. F. J. "Muonium Substituted Molecules." In Springer Proceedings in Physics, 229–44. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-76370-0_17.

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Gutowski, J. "ZnS: muonium data." In New Data and Updates for IV-IV, III-V, II-VI and I-VII Compounds, their Mixed Crystals and Diluted Magnetic Semiconductors, 628. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14148-5_348.

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Gutowski, J. "ZnSe: muonium data." In New Data and Updates for IV-IV, III-V, II-VI and I-VII Compounds, their Mixed Crystals and Diluted Magnetic Semiconductors, 634. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14148-5_353.

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Horváth, D. "Exotic Atoms and Muonium." In Handbook of Nuclear Chemistry, 1485–513. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-0720-2_28.

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Ansaldo, E. J., J. J. Boyle, Ch Niedermayer, G. D. Morris, J. H. Brewer, C. E. Stronach, and R. S. Cary. "Formation of Muonium and A Muonic Radical in Fullerene." In Physics and Chemistry of Finite Systems: From Clusters to Crystals, 1305–9. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-017-2645-0_180.

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Gutowski, J., K. Sebald, and T. Voss. "ZnSe: deep impurities, muonium data." In New Data and Updates for III-V, II-VI and I-VII Compounds, 459–60. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-92140-0_339.

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Gutowski, J., K. Sebald, and T. Voss. "ZnS: deep impurities, muonium data." In New Data and Updates for III-V, II-VI and I-VII Compounds, 477–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-92140-0_353.

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Conference papers on the topic "MUONIUM"

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MARCIANO, WILLIAM J. "MUONIUM LIFETIME AND HEAVY QUARK DECAYS (LESSONS LEARNED FROM MUONIUM)." In Proceedings of the Memorial Symposium in Honor of Vernon Willard Hughes. WORLD SCIENTIFIC, 2004. http://dx.doi.org/10.1142/9789812702425_0004.

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Olin, Arthur. "Thermal muonium in vacuum." In AIP Conference Proceedings Volume 150. AIP, 1986. http://dx.doi.org/10.1063/1.36137.

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Kirch, K. "Slow Muons and Muonium." In Seventh Meeting on CPT and Lorentz Symmetry. WORLD SCIENTIFIC, 2017. http://dx.doi.org/10.1142/9789813148505_0014.

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PREPOST, RICHARD. "MUONIUM-THE EARLY EXPERIMENTS." In Proceedings of the Memorial Symposium in Honor of Vernon Willard Hughes. WORLD SCIENTIFIC, 2004. http://dx.doi.org/10.1142/9789812702425_0003.

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Forslund, Ola Kenji. "Your Muonium is μ-drogen." In Proceedings of the 14th International Conference on Muon Spin Rotation, Relaxation and Resonance (μSR2017). Journal of the Physical Society of Japan, 2018. http://dx.doi.org/10.7566/jpscp.21.011066.

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Kaplan, Daniel, Derrick Mancini, James Phillips, Thomas Phillips, Thomas Roberts, KLAUS KIRCH, and Robert Reasenberg. "Measuring Antimatter Gravity with Muonium." In 38th International Conference on High Energy Physics. Trieste, Italy: Sissa Medialab, 2017. http://dx.doi.org/10.22323/1.282.0719.

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Dudnikov, V., and A. Dudnikov. "Ultracold muonium negative ion production." In SIXTH INTERNATIONAL SYMPOSIUM ON NEGATIVE IONS, BEAMS AND SOURCES (NIBS 2018). Author(s), 2018. http://dx.doi.org/10.1063/1.5083774.

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Cox, S. F. J. "Hydrogen In Oxides, Modelled By Muonium." In PHYSICS OF SEMICONDUCTORS: 27th International Conference on the Physics of Semiconductors - ICPS-27. AIP, 2005. http://dx.doi.org/10.1063/1.1994059.

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EIDES, MICHAEL I., and VALERY A. SHELYUTO. "HYPERFINE SPLITTING IN MUONIUM AND POSITRONIUM." In The Memorial Workshop Devoted to the 85th Birthday of V N Gribov. WORLD SCIENTIFIC, 2016. http://dx.doi.org/10.1142/9789813141704_0034.

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Kaplan, Daniel M., Klaus Kirch, Derrick C. Mancini, James D. Phillips, Thomas J. Phillips, Robert D. Reasenberg, Thomas J. Roberts, and Jeff Terry. "Progress Towards a Muonium Gravity Experiment." In Seventh Meeting on CPT and Lorentz Symmetry. WORLD SCIENTIFIC, 2017. http://dx.doi.org/10.1142/9789813148505_0064.

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Reports on the topic "MUONIUM"

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Hughes, V. W. Medium Energy Particle Physics - Muonium/RHIC - SPIN. Office of Scientific and Technical Information (OSTI), May 2003. http://dx.doi.org/10.2172/836598.

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Kuang, Yunan. Observation of the negative muonium ion in vacuum. Office of Scientific and Technical Information (OSTI), May 1989. http://dx.doi.org/10.2172/6141306.

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Matthias, B. E. A new search for conversion of muonium to antimuonium. Office of Scientific and Technical Information (OSTI), October 1991. http://dx.doi.org/10.2172/5131986.

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Yale, Bradley. Heavy Photon Displaced Vertex Search at 2.3GeV with Prospects for True Muonium Discovery. Office of Scientific and Technical Information (OSTI), September 2019. http://dx.doi.org/10.2172/1574119.

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Melnikov, Kirill. O(alpha{sup 3} ln(alpha)) Corrections to Muonium and Positronium Hyperfine Splitting. Office of Scientific and Technical Information (OSTI), July 2001. http://dx.doi.org/10.2172/784957.

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Kettell, S. H. Measurement of the 2 sup 2 S sub 1/2 -2 sup 2 P sub 3/2 fine structure interval in muonium. Office of Scientific and Technical Information (OSTI), August 1990. http://dx.doi.org/10.2172/6849854.

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Spencer, Matthew Brandon. A Measurement of the Muonic Dalitz Decay of the Neutral Kaon. Office of Scientific and Technical Information (OSTI), January 1995. http://dx.doi.org/10.2172/1423668.

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Jacot-Guillarmod, R., J. M. Bailey, G. A. Beer, P. E. Knowles, G. R. Mason, A. Olin, J. L. Beveridge, et al. Detection of hot muonic hydrogen atoms emitted in vacuum using x-rays. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/10154607.

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Hu, Chi-yu. Muonic molecular structure,. mu. -sticking probability and fusion rates for muon catalyzed fusion. Office of Scientific and Technical Information (OSTI), April 1990. http://dx.doi.org/10.2172/7132734.

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Kløcker Larsen, Rasmus. ”De kör över en ändå…”: Konsekvenser av gruvan i Kaunisvaara för Muonio sameby. Stockholm Environment Institute, April 2021. http://dx.doi.org/10.51414/sei2021.002.

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