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Yutaka Matsumi

Bio: Yutaka Matsumi is an academic researcher from Nagoya University. The author has contributed to research in topics: Photodissociation & Laser-induced fluorescence. The author has an hindex of 37, co-authored 215 publications receiving 4730 citations. Previous affiliations of Yutaka Matsumi include Hokkaido University & University of Southern Denmark.


Papers
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TL;DR: In this article, the relative signal peak area of various target species in the LISPA-MS spectra was calculated as the ion-signal fraction of the species relative to the total signal peak areas summed over all the ion peaks in each spectrum.
Abstract: Particle mass spectrometers of two types—a time-of-flight aerosol mass spectrometer (AMS) of Aerodyne Research Inc. and a laser desorption/ionization single particle aerosol mass spectrometer (LISPA-MS) developed at Nagoya University—were deployed to characterize aerosol particles in the Tokyo metropolitan area during the summer of 2008. Based on the ensemble measurements by AMS, equivalent mass concentration of organic aerosol, traced by mass-to-charge ratio (m/z) 44, showed a closer correlation with particulate nitrate and gas-phase odd oxygen, [O 3 +NO 2 ], whereas equivalent mass concentration of organic aerosol, traced by m/z 57, did not. On a particle-by-particle basis, the relative signal peak area of various target species in the LISPA-MS spectra, which was calculated as the ion-signal fraction of the species relative to the total signal peak area summed over all the ion peaks in each spectrum, was used as a measure of the relative amount of the species. A rough qualitative agreement was obtained ...

13 citations

Journal ArticleDOI
TL;DR: In this paper, the branching ratio for CF 3 ONO 2 formation is k 5b /(k 5a +k 5b )=(1.67±0.27)×10 −2.

13 citations

Journal ArticleDOI
TL;DR: In this paper, an experimental and theoretical study of the formation of hydrogen atom in the photolysis of acetone at 193 nm is reported, where the H atom photofragments are detected by the technique of vacuum ultraviolet laser-induced fluorescence (VUV-LIF) spectroscopy at 121.6 nm.
Abstract: An experimental and theoretical study of the formation of hydrogen atom in the photolysis of acetone at 193 nm is reported. The H atom photofragments are detected by the technique of vacuum ultraviolet laser-induced fluorescence (VUV-LIF) spectroscopy at 121.6 nm. The quantum yield for H atom formation from acetone photolysis at 193 nm is determined to be 0.039 ′ 0.006. The Doppler profiles of the H atom photofragments are measured by scanning the probe laser wavelength around the resonance frequency of the H atom at 121.6 nm. The nascent kinetic energy distribution of the H atom fragments is found to be characterized by a Maxwell-Boltzmann function with the temperature of 5000 K. The spatially isotropic recoil distribution in the H atom photofragmentation is observed. The potential energy surfaces for the H atom formation processes from acetone photolysis are examined using molecular orbital calculation methods. Atmospheric implications of the present result are briefly discussed.

13 citations


Cited by
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TL;DR: In this paper, the photodissociation processes occurring in molecular oxygen following the two-photon 3dπ(3Σ1g −) Rydberg excitation around 225 nm are presented to show the improvement in spatial resolution in the ion and electron images.
Abstract: The application of electrostatic lenses is demonstrated to give a substantial improvement of the two-dimensional (2D) ion/electron imaging technique. This combination of ion lens optics and 2D detection makes “velocity map imaging” possible, i.e., all particles with the same initial velocity vector are mapped onto the same point on the detector. Whereas the more common application of grid electrodes leads to transmission reduction, severe trajectory deflections and blurring due to the non-point source geometry, these problems are avoided with open lens electrodes. A three-plate assembly with aperture electrodes has been tested and its properties are compared with those of grid electrodes. The photodissociation processes occurring in molecular oxygen following the two-photon 3dπ(3Σ1g −)(v=2, N=2)←X(3Σg −) Rydberg excitation around 225 nm are presented here to show the improvement in spatial resolution in the ion and electron images. Simulated trajectory calculations show good agreement with experiment and ...

2,430 citations

Journal ArticleDOI
TL;DR: An overview of PFASs detected in the environment, wildlife, and humans, and recommend clear, specific, and descriptive terminology, names, and acronyms for PFAS, can be found in this article.
Abstract: The primary aim of this article is to provide an overview of perfluoroalkyl and polyfluoroalkyl substances (PFASs) detected in the environment, wildlife, and humans, and recommend clear, specific, and descriptive terminology, names, and acronyms for PFASs. The overarching objective is to unify and harmonize communication on PFASs by offering terminology for use by the global scientific, regulatory, and industrial communities. A particular emphasis is placed on long-chain perfluoroalkyl acids, substances related to the long-chain perfluoroalkyl acids, and substances intended as alternatives to the use of the long-chain perfluoroalkyl acids or their precursors. First, we define PFASs, classify them into various families, and recommend a pragmatic set of common names and acronyms for both the families and their individual members. Terminology related to fluorinated polymers is an important aspect of our classification. Second, we provide a brief description of the 2 main production processes, electrochemical fluorination and telomerization, used for introducing perfluoroalkyl moieties into organic compounds, and we specify the types of byproducts (isomers and homologues) likely to arise in these processes. Third, we show how the principal families of PFASs are interrelated as industrial, environmental, or metabolic precursors or transformation products of one another. We pay particular attention to those PFASs that have the potential to be converted, by abiotic or biotic environmental processes or by human metabolism, into long-chain perfluoroalkyl carboxylic or sulfonic acids, which are currently the focus of regulatory action. The Supplemental Data lists 42 families and subfamilies of PFASs and 268 selected individual compounds, providing recommended names and acronyms, and structural formulas, as well as Chemical Abstracts Service registry numbers. Integr Environ Assess Manag 2011;7:513–541. © 2011 SETAC

2,356 citations

Journal Article
TL;DR: Denman et al. as discussed by the authors presented the Couplings between changes in the climate system and biogeochemistry Coordinating Lead Authors: Kenneth L. Denman (Canada), Guy Brasseur (USA, Germany), Amnat Chidthaisong (Thailand), Philippe Ciais (France), Peter M. Cox (UK), Robert E. Austin (USA), D.B. Wofsy (USA) and Xiaoye Zhang (China).
Abstract: Couplings Between Changes in the Climate System and Biogeochemistry Coordinating Lead Authors: Kenneth L. Denman (Canada), Guy Brasseur (USA, Germany) Lead Authors: Amnat Chidthaisong (Thailand), Philippe Ciais (France), Peter M. Cox (UK), Robert E. Dickinson (USA), Didier Hauglustaine (France), Christoph Heinze (Norway, Germany), Elisabeth Holland (USA), Daniel Jacob (USA, France), Ulrike Lohmann (Switzerland), Srikanthan Ramachandran (India), Pedro Leite da Silva Dias (Brazil), Steven C. Wofsy (USA), Xiaoye Zhang (China) Contributing Authors: D. Archer (USA), V. Arora (Canada), J. Austin (USA), D. Baker (USA), J.A. Berry (USA), R. Betts (UK), G. Bonan (USA), P. Bousquet (France), J. Canadell (Australia), J. Christian (Canada), D.A. Clark (USA), M. Dameris (Germany), F. Dentener (EU), D. Easterling (USA), V. Eyring (Germany), J. Feichter (Germany), P. Friedlingstein (France, Belgium), I. Fung (USA), S. Fuzzi (Italy), S. Gong (Canada), N. Gruber (USA, Switzerland), A. Guenther (USA), K. Gurney (USA), A. Henderson-Sellers (Switzerland), J. House (UK), A. Jones (UK), C. Jones (UK), B. Karcher (Germany), M. Kawamiya (Japan), K. Lassey (New Zealand), C. Le Quere (UK, France, Canada), C. Leck (Sweden), J. Lee-Taylor (USA, UK), Y. Malhi (UK), K. Masarie (USA), G. McFiggans (UK), S. Menon (USA), J.B. Miller (USA), P. Peylin (France), A. Pitman (Australia), J. Quaas (Germany), M. Raupach (Australia), P. Rayner (France), G. Rehder (Germany), U. Riebesell (Germany), C. Rodenbeck (Germany), L. Rotstayn (Australia), N. Roulet (Canada), C. Sabine (USA), M.G. Schultz (Germany), M. Schulz (France, Germany), S.E. Schwartz (USA), W. Steffen (Australia), D. Stevenson (UK), Y. Tian (USA, China), K.E. Trenberth (USA), T. Van Noije (Netherlands), O. Wild (Japan, UK), T. Zhang (USA, China), L. Zhou (USA, China) Review Editors: Kansri Boonpragob (Thailand), Martin Heimann (Germany, Switzerland), Mario Molina (USA, Mexico) This chapter should be cited as: Denman, K.L., G. Brasseur, A. Chidthaisong, P. Ciais, P.M. Cox, R.E. Dickinson, D. Hauglustaine, C. Heinze, E. Holland, D. Jacob, U. Lohmann, S Ramachandran, P.L. da Silva Dias, S.C. Wofsy and X. Zhang, 2007: Couplings Between Changes in the Climate System and Biogeochemistry. In: Climate Change 2007: The Physical Science Basis. Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change [Solomon, S., D. Qin, M. Manning, Z. Chen, M. Marquis, K.B. Averyt, M.Tignor and H.L. Miller (eds.)]. Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA.

2,208 citations