Homogeneous Charge Compression Ignition Combustion of Dimethyl Ether

Total Page:16

File Type:pdf, Size:1020Kb

Homogeneous Charge Compression Ignition Combustion of Dimethyl Ether Downloaded from orbit.dtu.dk on: Oct 04, 2021 Homogeneous Charge Compression Ignition Combustion of Dimethyl Ether Pedersen, Troels Dyhr Publication date: 2011 Document Version Publisher's PDF, also known as Version of record Link back to DTU Orbit Citation (APA): Pedersen, T. D. (2011). Homogeneous Charge Compression Ignition Combustion of Dimethyl Ether. Technical University of Denmark. General rights Copyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. Users may download and print one copy of any publication from the public portal for the purpose of private study or research. You may not further distribute the material or use it for any profit-making activity or commercial gain You may freely distribute the URL identifying the publication in the public portal If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. - 1 - - Homogeneous Charge Compression Ignition Combustion of Dimethyl Ether PhD Thesis Troels Dyhr Pedersen DTU Mechanical Engineering Department of Mechanical Engineering - 2 - - Table of contents 1 FOREWORD 6 2 NOMENCLATURE 7 3 RÉSUMÉ 8 4 RESUMÉ (DANSK) 10 5 INTRODUCTION 12 5.1 About HCCI combustion 12 5.2 Background of this project 13 5.3 Scope of investigation 14 5.3.1 The study on combustion phasing 14 5.3.2 The study on combustion noise 15 6 THE BASICS OF HCCI COMBUSTION 16 6.1 Combustion principle 16 6.2 Combustion characteristics 16 6.3 Combustion phasing parameters 17 6.3.1 Compression ratio 17 6.3.2 Equivalence ratio 17 6.3.3 Inlet temperature 17 6.3.4 Exhaust gas recirculation 17 6.4 Thermal efficiency 18 6.5 Emission characteristics 18 7 COMBUSTION OF DME 20 7.1 Combustion stoichiometry 20 7.2 Physical and chemical properties of DME 20 7.3 Development in the use of dimethyl ether as a fuel 21 8 DESCRIPTION OF EXPERIMENTAL ENGINE SETUP 22 8.1 Engine 22 - 3 - - 8.1.1 Engine setup 22 8.1.2 Modifications 22 8.1.3 Piston modifications 24 8.2 Cylinder pressure transducers 25 8.3 Data acquisition 25 9 HEAT RELEASE CALCULATIONS 27 9.1 The Heat Release analysis 27 9.2 Location of TDC 27 9.3 Specific heat ratio 29 9.4 Temperature estimate 31 9.5 Heat losses 31 10 THE REACTION KINETICS OF DME 33 10.1 Elementary reaction model 33 10.2 The detailed reaction scheme 33 10.3 Reducing the mechanism for lean combustion 33 10.4 Comparison of the full and the reduced schemes 36 10.5 Reaction paths 37 10.5.1 Initiation and low temperature reaction paths 37 10.5.2 High temperature reactions 41 10.6 Manipulating low temperature reactions 42 10.6.1 Effect of methanol on low temperature reactions 42 10.6.2 Effect of EGR 43 10.7 List of species 44 11 ENGINE ACOUSTICS 45 11.1 Measurements 45 11.2 Choice of sampling frequency 45 11.3 Equipment 46 11.4 Handling the confined space acoustic issues 46 11.5 Post sample digital filtering 47 11.5.1 Filter methodology 47 11.5.2 Filtering of pressure data for heat release analysis 47 - 4 - - 11.5.3 Filtering of sample data for frequency analysis 48 11.6 Representation of acoustic measurements 48 11.6.1 Sound pressure 48 11.6.2 Sound pressure level 48 11.6.3 Time domain representation 49 11.6.4 Frequency domain representation 50 11.6.5 Frequency spectrum analysis in the time domain 51 11.7 Theory of cylinder acoustics 53 11.7.1 Circumferential modes 53 11.7.2 Radial modes 53 11.7.3 Axial modes 54 11.8 Calculation of resonance frequencies 54 11.9 COMSOL calculations of cylinder acoustic resonance 55 12 SIMULATION OF DETONATION PHENOMENA 58 12.1 Background 58 12.2 Explosions 59 12.2.1 Uniform explosion 59 12.2.2 Non uniform explosions and pressure wave amplification 59 12.3 Detonations 60 12.3.1 Introduction 60 12.3.2 Detonation waves 61 12.3.3 Shock wave 61 12.3.4 Reference for velocitities 61 12.3.5 Conservation equations 63 12.3.6 The Rayleigh relation 63 12.3.7 The Hugoniot relation 64 12.3.8 Determination of the Chapman Jouget velocity 67 12.3.9 Results for the stationary solution 70 12.4 Detonation study in CFD 71 12.4.1 Problem setup in STAR-CD 71 12.4.2 Simulation results 73 12.5 Observations of detonation in HCCI combustion 76 12.5.1 Experimental setup 76 12.5.2 Pressure trace 77 13 SUMMARY AND CONCLUSION 79 14 REFERENCES 81 15 APPENDIX A: REDUCED SCHEME FOR LEAN PREMIXED DME COMBUSTION 84 - 5 - - 16 APPENDIX B: DETONATION MODEL IN EES 86 17 PAPER I : THE EFFECT OF COMPRESSION RATIO, EQUIVALENCE RATIO AND ENGINE SPEED ON HCCI COMBUSTION OF DIMETHYL ETHER 86 18 PAPER II: CONTROLLING THE HEAT RELEASE OF DME HCCI COMBUSTION WITH METHANOL AND EGR 89 19 PAPER III: REDUCING HCCI COMBUSTION NOISE THROUGH PISTON DESIGN 90 - 6 - - 1 Foreword The work described in this thesis was initiated in June 2006 and completed in January 2010. It was carried out under supervision of associate professor Jesper Schramm at the Department of Mechanical Engineering, Technical University of Denmark. I wish to thank Jesper Schramm for offering me the PhD position. I also wish to thank the rest of the Internal Combustion Engine Group. Everyone has been supportive and helpful in many situations. In 2008 I visited the National Traffic Safety and Environmental Laboratories in Tokyo, Japan, for 5 months. The purpose of the visit was to perform experiments with HCCI combustion on a truck engine test bench. I am grateful for having been given this opportunity to work in a professional environment, and wish to thank the people whom I worked with at NTSEL for their help and kindness. - 7 - - 2 Nomenclature AC Alternating Current ASRT Automatic Scheme Reduction Tool ATAC Active Thermo Atmosphere Combustion ATDC After Top Dead Center BMEP Brake Mean Effective Pressure BTDC Before Top Dead Center CAI Controlled Auto Ignition CCI Combined Combustion System CFD Computational Fluid Dynamics CI Compression Ignition CJ Chapman Jouget DFT Discrete Fourier Transform DI Direct Injection DME Dimethyl Ether EGR Exhaust Gas Recirculation FIR Finite Impulse Response FFT Fast Fourier Transform GCI Gasoline Compression Ignition HCCI Homogenous Charge Compression Ignition HTR High Temperature Reactions IIR Infinite Impulse Response IMEP Indicated Mean Effective Pressure LHV Lower Heating Value LTR Low Temperature Reactions NTSEL National Traffic Safety and Environment Laboratories PCCI Premixed Charge Compression Ignition PCI Premixed Compression Ignition RMS Root Mean Square SI Spark Ignition SPL Sound Pressure Level TDC Top Dead Center ZND Zel´dovich Neumann Döring - 8 - - 3 Résumé This thesis is based on experimental and numerical studies on the use of dimethyl ether (DME) in the homogeneous charge compression ignition (HCCI) combustion process. The first paper in this thesis was published in 2007 and describes HCCI combustion of pure DME in a small diesel engine. The tests were designed to investigate the effect of engine speed, compression ratio and equivalence ratio on the combustion timing and the engine performance. It was found that the required compression ratio depended on the equivalence ratio used. A lower equivalence ratio requires a higher compression ratio before the fuel is burned completely, due to lower in-cylinder temperatures and lower reaction rates. The study provided some insight in the importance of operating at the correct compression ratio, as well as the operational limitations and emission characteristics of HCCI combustion. HCCI combustion process is governed mainly by chemical kinetics. To understand the combustion process therefore requires detailed knowledge of the dominating reaction paths in lean premixed combustion of DME. The reactions were studied by running simulations of HCCI combustion in CHEMKIN II [1] with a detailed reaction mechanism for DME developed at Lawrence Livermore National Laboratory in 2004 [2]. The dominating reactions paths were then identified and used to create a simple reaction mechanism containing 55 reactions only. It contains just enough reactions to successfully predict ignition as well as low and high temperature reactions with reasonable similarity to the original mechanism. By reducing the mechanism to its essential reactions it becomes more useful to CFD models of HCCI combustion. The number of elementary reactions has a great influence on computational demands and computing time, so the use of a simple mechanism greatly reduces both. Reaction paths for methanol and methane were included amongst the elementary reactions, since these two fuels are commonly used to control the radical behavior in the initial phase of combustion and hence the combustion phasing of the fuel in an engine, as well as enabling an increase in engine power. The use of methanol for combustion phasing control was tested successfully in a large diesel engine with common rail, in which the piston bowls were widened to give a compression ratio of 14.5. This compression ratio still allows DI CI operation with DME, but requires a substantial combustion delay in HCCI operation with DME to achieve post TDC combustion. By adding methanol to the inlet port during HCCI combustion of DME, the engine reached 50 percent of its full DI CI load capability without engine knock at 1000 rpm and somewhat less at 1800 rpm. The engine also had EGR capability which was used to demonstrate the effect on HCCI combustion phasing of increasing EGR ratios.
Recommended publications
  • A Chemical Kinetics Network for Lightning and Life in Planetary Atmospheres P
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by St Andrews Research Repository The Astrophysical Journal Supplement Series, 224:9 (33pp), 2016 May doi:10.3847/0067-0049/224/1/9 © 2016. The American Astronomical Society. All rights reserved. A CHEMICAL KINETICS NETWORK FOR LIGHTNING AND LIFE IN PLANETARY ATMOSPHERES P. B. Rimmer and Ch Helling School of Physics and Astronomy, University of St Andrews, St Andrews, KY16 9SS, UK; [email protected] Received 2015 June 3; accepted 2015 October 22; published 2016 May 23 ABSTRACT There are many open questions about prebiotic chemistry in both planetary and exoplanetary environments. The increasing number of known exoplanets and other ultra-cool, substellar objects has propelled the desire to detect life andprebiotic chemistry outside the solar system. We present an ion–neutral chemical network constructed from scratch, STAND2015, that treats hydrogen, nitrogen, carbon, and oxygen chemistry accurately within a temperature range between 100 and 30,000 K. Formation pathways for glycine and other organic molecules are included. The network is complete up to H6C2N2O3. STAND2015 is successfully tested against atmospheric chemistry models for HD 209458b, Jupiter, and the present-day Earth using a simple one- dimensionalphotochemistry/diffusion code. Our results for the early Earth agree with those of Kasting for CO2,H2, CO, and O2, but do not agree for water and atomic oxygen. We use the network to simulate an experiment where varied chemical initial conditions are irradiated by UV light. The result from our simulation is that more glycine is produced when more ammonia and methane is present.
    [Show full text]
  • Oxidation of Organic Compounds Present in Fuels Under Conditions of Interest for Combustion Processes
    2019 22 Lorena Marrodán Bretón Oxidation of organic compounds present in fuels under conditions of interest for combustion processes Departamento Ingeniería Química y Tecnologías del Medio Ambiente Director/es MILLERA PERALTA, ÁNGELA ALZUETA ANIA, MARIA UJUE Reconocimiento – NoComercial – © Universidad de Zaragoza SinObraDerivada (by-nc-nd): No se Servicio de Publicaciones permite un uso comercial de la obra original ni la generación de obras derivadas. ISSN 2254-7606 Tesis Doctoral OXIDATION OF ORGANIC COMPOUNDS PRESENT IN FUELS UNDER CONDITIONS OF INTEREST FOR COMBUSTION PROCESSES Autor Lorena Marrodán Bretón Director/es MILLERA PERALTA, ÁNGELA ALZUETA ANIA, MARIA UJUE UNIVERSIDAD DE ZARAGOZA Ingeniería Química y Tecnologías del Medio Ambiente 2018 Repositorio de la Universidad de Zaragoza – Zaguan http://zaguan.unizar.es “Oxidation of organic compounds present in fuels under conditions of interest for combustion processes” This dissertation is submitted to the Department of Chemical Engineering and Environmental Technologies at the University of Zaragoza (Spain) in fulfillment of the requirements for the degree of Doctor Lorena Marrodán Bretón Zaragoza, 2018 Dña. María Ujué Alzueta Anía, Catedrática de Universidad, y Dña. Ángela Millera Peralta, Profesora Titular del Departamento de Ingeniería Química y Tecnologías del Medio Ambiente de la Universidad de Zaragoza, INFORMAN Que la presente memoria titulada: “Oxidation of organic compounds present in fuels under conditions of interest for combustion processes” ha sido realizada bajo
    [Show full text]
  • LIBRARIES Archives M.S
    Automated reaction mechanism generation: Data collaboration, Heteroatom implementation, and Model validation by MASSACHUSETTS INSTITUTE Michael Richard Harper, Jr. OF TECHNOLOGY JUN 13 21011 B.S. in Chemical Engineering University of California, Berkeley (2005) K--LIBRARIES ARCHiVES M.S. in Chemical Engineering Practice Massachusetts Institute of Technology (2007) Submitted to the Department of Chemical Engineering in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY IN CHEMICAL ENGINEERING at the MASSACHUSETTS INSTITUTE OF TECHNOLOGY June 2011 © 2011 Massachusetts Institute of Technology. All rights reserved. Signature of Author: )epartmen< of Chemical Engineering Date: May 10, 2011 Certified by: _ Hoy William H. Green Hoyt C. ~tel Professor of Chemical Engineering Thesis Supervisor Accepted by: William M. Deen Carbon P. Dubbs Professor of Chemical Engineering Chairman, Committee for Graduate Students 2 Automated Reaction Mechanism Generation: Data Collaboration, Heteroatom Implementation and Model Validation by Michael R. Harper Jr. Submitted to the Department of Chemical Engineering on May 10, 2011 in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy in Chemical Engineering ABSTRACT Nearly two-thirds of the United States' transportation fuels are derived from non-renewable fossil fuels. This demand of fossil fuels requires the United States to import ~ 60% of its total fuel consumption. Relying so heavily on foreign oil is a threat to national security, not to mention that burning all of these fossil fuels produces increased levels of C0 2, a greenhouse gas that contributes to global warming. This is not a sustainable model. The United States government has recently passed legislation that requires greenhouse gas emissions to be reduced to 80% of the 2005 level by the year 2050.
    [Show full text]
  • Ph. D. Thesis David Schlereth, M.Sc
    TECHNISCHE UNIVERSITÄT MÜNCHEN Department Chemie Lehrstuhl I für Technische Chemie Kinetic and Reactor Modeling for the Methanation of Carbon Dioxide David Schlereth Vollständiger Abdruck der von der Fakultät für Chemie der Technischen Universität München zur Erlangung des akademischen Grades eines Doktor der Naturwissenschaften (Dr. rer. nat.) genehmigten Dissertation. Vorsitzender: Univ.-Prof. Dr. T. Brück Prüfer der Dissertation: 1. Univ.-Prof. Dr. K.-O. Hinrichsen 2. Univ.-Prof. Dr. K. Köhler 3. Univ.-Prof. Dr. K. Reuter Die Dissertation wurde am 02.03.2015 bei der Technischen Universität München einge- reicht und durch die Fakultät für Chemie am 28.04.2015 angenommen. Acknowledgments There have been so many people who contributed to this work, may it be in scientific or non-scientific ways. I would like to thank all, who have supported or helped in either way during the last years. I would like to thank Prof. Dr.-Ing. Kai-Olaf Hinrichsen, first of all for the opportunity to work in his group on this interesting topic. I appreciate the given freedom and trust of letting me direct my work according to my interests, his supervision, and steady interest in my work as well as the given opportunities to present our results on conferences. The last three years would have never been the same without my colleagues. Working atmosphere and cooperativeness could not have been better and might be unique at the Chair of Chemical Engineering. Thanks to all of you for this throughout the years! I would also not have missed our non-scientific leisure activities. I would like also to thank Tassilo von Aretin, Matthias Fichtl and Franz Koschany, who have always been open for discussion and brought up new ideas and solutions.
    [Show full text]
  • Orbital Evolution, Activity, and Mass Loss of Comet C/1995 O1 (Hale
    Version September 12, 2017 Preprint typeset using LATEX style emulateapj v. 08/22/09 ORBITAL EVOLUTION, ACTIVITY, AND MASS LOSS OF COMET C/1995 O1 (HALE-BOPP). I. CLOSE ENCOUNTER WITH JUPITER IN THIRD MILLENNIUM BCE AND EFFECTS OF OUTGASSING ON THE COMET’S MOTION AND PHYSICAL PROPERTIES Zdenek Sekanina1 & Rainer Kracht2 1Jet Propulsion Laboratory, California Institute of Technology, 4800 Oak Grove Drive, Pasadena, CA 91109, U.S.A. 2Ostlandring 53, D-25335 Elmshorn, Schleswig-Holstein, Germany Version September 12, 2017 ABSTRACT This comprehensive study of comet C/1995 O1 focuses first on investigating its orbital motion over a period of 17.6 yr (1993–2010). The comet is suggested to have approached Jupiter to 0.005 AU on 2251 November 7, in general conformity with Marsden’s (1999) proposal of a Jovian encounter nearly 4300− yr ago. The variations of sizable nongravitational effects with heliocentric distance correlate with the evolution of outgassing, asymmetric relative to perihelion. The future orbital period will shorten to 1000 yr because of orbital-cascade resonance effects. We find that the sublimation curves of parent molecules∼ are fitted with the type of a law used for the nongravitational acceleration, determine their orbit-integrated mass loss, and conclude that the share of water ice was at most 57%, and possibly less than 50%, of the total outgassed mass. Even though organic parent molecules (many still unidentified) had very low abundances relative to water individually, their high molar mass and sheer number made them, summarily, important potential mass contributors to the total production of gas. The mass loss of dust per orbit exceeded that of water ice by a factor of 12, a dust loading high enough to imply a major role for heavy organic molecules of low volatility in∼ accelerating the minuscule dust particles in the expanding halos to terminal velocities as high as 0.7 km s−1.
    [Show full text]
  • Formation and High-Order Carboxylic Acids (RCOOH) in Interstellar Analogous Ices of Carbon Dioxide (CO2) and Methane(CH4) Cheng Zhu1,2, Andrew M
    The Astrophysical Journal Supplement Series, 234:15 (13pp), 2018 January https://doi.org/10.3847/1538-4365/aa9f28 © 2018. The American Astronomical Society. All rights reserved. Formation and High-order Carboxylic Acids (RCOOH) in Interstellar Analogous Ices of Carbon Dioxide (CO2) and Methane(CH4) Cheng Zhu1,2, Andrew M. Turner1,2, Matthew J. Abplanalp1,2, and Ralf I. Kaiser1,2 1 Department of Chemistry, University of Hawaii at Mânoa, Honolulu, HI 96822, USA; [email protected] 2 W.M. Keck Laboratory in Astrochemistry, University of Hawaii at Mânoa, Honolulu, HI 96822, USA Received 2017 October 10; revised 2017 November 13; accepted 2017 November 30; published 2018 January 16 Abstract This laboratory study simulated the abiotic formation of carboxylic acids (RCOOH) in interstellar analogous ices of carbon dioxide (CO2) and methane (CH4) at 10 K upon exposure to energetic electrons. The chemical processing of the ices and the subsequent warm-up phase were monitored online and in situ, exploiting Fourier Transform Infrared Spectrometry and quadrupole mass spectrometry. Characteristic absorptions of functional groups of carboxylic acids (RCOOH) were observed in the infrared spectra of the irradiated ice. Two proposed reaction mechanisms replicated the kinetic profiles of the carboxylic acids along with the decay profile of the precursors during the irradiation via hydrocarbon formation, followed by carboxylation and/or through acetic acid along with mass growth processes of the alkyl chain. Mass spectra recorded during the warm-up phase demonstrated that these acids are distributed from acetic acid (CH3COOH) up to decanoic acid (C9H19COOH). High-dose irradiation studies (91±14 eV) converted low-molecular-weight acids such as acetic acid (CH3COOH) and propionic acid (C2H5COOH) to higher-molecular-weight carboxylic acids, compared to low-dose irradiation studies (18±3eV).
    [Show full text]
  • Classic and Advanced Ceramics: from Fundamentals to Applications
    Robert B. Heimann Classic and Advanced Ceramics From Fundamentals to Applications Robert B. Heimann Classic and Advanced Ceramics Related Titles Aldinger, F., Weberruss, V. A. Volume 4: Applications Advanced Ceramics and 2012 Future Materials Hardcover ISBN: 978-3-527-31158-3 An Introduction to Structures, Properties and Technologies Öchsner, A., Ahmed, W. (eds.) 2010 Hardcover Biomechanics of Hard Tissues ISBN: 978-3-527-32157-5 Modeling, Testing, and Materials 2010 Riedel, R., Chen, I-W. (eds.) Hardcover Ceramics Science and ISBN: 978-3-527-32431-6 Technology 4 Volume Set Krenkel, W. (ed.) Hardcover Ceramic Matrix Composites ISBN: 978-3-527-31149-1 Fiber Reinforced Ceramics and their Applications Volume 1: Structures 2008 Hardcover 2008 ISBN: 978-3-527-31361-7 Hardcover ISBN: 978-3-527-31155-2 Öchsner, A., Murch, G. E., de Lemos, M. J. S. (eds.) Volume 2: Properties Cellular and Porous Materials 2010 Hardcover Thermal Properties Simulation and Prediction ISBN: 978-3-527-31156-9 2008 Hardcover ISBN: 978-3-527-31938-1 Volume 3: Synthesis and Processing 2010 Hardcover ISBN: 978-3-527-31157-6 Robert B. Heimann Classic and Advanced Ceramics From Fundamentals to Applications The Author All books published by Wiley-VCH are carefully produced. Nevertheless, authors, editors, and Prof. Dr. Robert B. Heimann publisher do not warrant the information Am Stadtpark 2A contained in these books, including this book, to 02826 Görlitz be free of errors. Readers are advised to keep in mind that statements, data, illustrations, procedural details or other items may inadvertently be inaccurate. Library of Congress Card No.: applied for British Library Cataloguing-in-Publication Data A catalogue record for this book is available from the British Library.
    [Show full text]
  • Catalysis Science & Technology
    Catalysis Science & Technology View Article Online MINI REVIEW View Journal | View Issue Recent advances in hydrogenation of CO2 into via Cite this: Catal. Sci. Technol.,2021, hydrocarbons methanol intermediate over 11,1665 heterogeneous catalysts Poonam Sharma, Joby Sebastian, Sreetama Ghosh, Derek Creaser and Louise Olsson * The efficient conversion of CO2 to hydrocarbons offers a way to replace the dependency on fossil fuels and mitigate the accumulation of surplus CO2 in the atmosphere that causes global warming. Therefore, various efforts have been made in recent years to convert CO2 to fuels and value-added chemicals. In this review, the direct and indirect hydrogenation of CO2 to hydrocarbons via methanol as an intermediate is spotlighted. We discuss the most recent approaches in the direct hydrogenation of CO2 into hydrocarbons via the methanol route wherein catalyst design, catalyst performance, and the reaction mechanism of CO2 hydrogenation are discussed in detail. As a comparison, various studies related to CO2 to methanol on Creative Commons Attribution-NonCommercial 3.0 Unported Licence. transition metals and metal oxide-based catalysts and methanol to hydrocarbons are also provided, and Received 29th September 2020, the performance of various zeolite catalysts in H2,CO2,andH2O rich environments is discussed during the Accepted 4th January 2021 conversion of methanol to hydrocarbons. In addition, a detailed analysis of the performance and mechanisms of the CO hydrogenation reactions is summarized based on different kinetic modeling DOI: 10.1039/d0cy01913e 2 studies. The challenges remaining in this field are analyzed and future directions associated with direct rsc.li/catalysis synthesis of hydrocarbons from CO2 are outlined.
    [Show full text]
  • JILA Team Identifies Missing Piece in How Fossil Fuel Combustion Contributes to Air Pollution 31 October 2016
    Green Car Congress: JILA team identifies missing piece in how fossil fue... http://www.greencarcongress.com/2016/10/20161031-jila.html 1 November 2016 Home Topics Archives About Contact RSS Headlines « Mercedes-BenzGreen Car Congress powering © 2016 ahead BioAge with Group, €3B strategicLLC. All Rights engine Reserved. initiative; | Home increasing | BioAge Group electrification, 48V; diesel and gasoline; cylinder deactivation | Main | Microchip introduces first automotive-grade LIN SiP with touch hardware support » Print this po st JILA team identifies missing piece in how fossil fuel combustion contributes to air pollution 31 October 2016 JILA physicists and colleagues have identified a long-missing piece in the puzzle of exactly how fossil fuel combustion contributes to air pollution and a warming climate. Performing chemistry experiments in a new way, they observed a key molecule that appears briefly during a common chemical reaction in the atmosphere. JILA a partnership of the National Institute of Standards and Technology (NIST) and the University of Colorado Boulder. Their paper appears in Science. The reaction combines the hydroxyl molecule (OH, produced by reaction of oxygen and water) and carbon monoxide (CO, a byproduct of incomplete fossil fuel combustion) to form hydrogen (H) and carbon dioxide (CO2). Artist’s conception of an infrared frequency comb “watching” the reaction of a molecule of carbon monoxide (CO, red and black) and hydroxyl radical (OD red and yellow) as they form the elusive reaction intermediate DOCO (red/black/red/yellow) before DOCO falls apart. This chemical reaction was seen for the first time under normal atmospheric conditions in the laboratory by the Ye group.
    [Show full text]
  • Hcooh) in Interstellar and Cometary Ices
    The Astrophysical Journal, 727:27 (15pp), 2011 January 20 doi:10.1088/0004-637X/727/1/27 C 2011. The American Astronomical Society. All rights reserved. Printed in the U.S.A. LABORATORY STUDIES ON THE FORMATION OF FORMIC ACID (HCOOH) IN INTERSTELLAR AND COMETARY ICES Chris J. Bennett1,2, Tetsuya Hama3,5, Yong Seol Kim1, Masahiro Kawasaki3, and Ralf I. Kaiser1,2,4 1 Department of Chemistry, University of Hawaii, Honolulu, HI 96822, USA; [email protected] 2 NASA Astrobiology Institute, University of Hawaii, Honolulu, HI 96822, USA 3 Department of Molecular Engineering, Kyoto University, Kyoto 615-8510, Japan Received 2010 July 9; accepted 2010 October 5; published 2010 December 29 ABSTRACT Mixtures of water (H2O) and carbon monoxide (CO) ices were irradiated at 10 K with energetic electrons to simulate the energy transfer processes that occur in the track of galactic cosmic-ray particles penetrating interstellar ices. We identified formic acid (HCOOH) through new absorption bands in the infrared spectra at 1690 and 1224 cm−1 (5.92 and 8.17 μm, respectively). During the subsequent warm-up of the irradiated samples, formic acid is evident from the mass spectrometer signal at the mass-to-charge ratio, m/z = 46 (HCOOH+) as the ice sublimates. The detection of formic acid was confirmed using isotopically labeled water-d2 with carbon monoxide, leading to formic acid-d2 (DCOOD). The temporal fits of the reactants, reaction intermediates, and products elucidate two reaction pathways to formic acid in carbon monoxide–water ices. The reaction is induced by unimolecular decomposition of water forming atomic hydrogen (H) and the hydroxyl radical (OH).
    [Show full text]
  • Kinetic and Multidimensional Transport Coupled Numerical Investigation of Nox Formation During Syngas and Natural Gas Combustion
    University of South Carolina Scholar Commons Theses and Dissertations Spring 2020 Kinetic and Multidimensional Transport Coupled Numerical Investigation of Nox Formation During Syngas and Natural Gas Combustion Sheikh Farhan Ahmed Follow this and additional works at: https://scholarcommons.sc.edu/etd Part of the Mechanical Engineering Commons Recommended Citation Ahmed, S. F.(2020). Kinetic and Multidimensional Transport Coupled Numerical Investigation of Nox Formation During Syngas and Natural Gas Combustion. (Doctoral dissertation). Retrieved from https://scholarcommons.sc.edu/etd/5672 This Open Access Dissertation is brought to you by Scholar Commons. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of Scholar Commons. For more information, please contact [email protected]. KINETIC AND MULTIDIMENSIONAL TRANSPORT COUPLED NUMERICAL INVESTIGATION OF NOX FORMATION DURING SYNGAS AND NATURAL GAS COMBUSTION by Sheikh Farhan Ahmed Bachelor of Science Bangladesh University of Engineering & Technology, 2008 Master of Science Bangladesh University of Engineering and Technology, 2010 Submitted in Partial Fulfillment of the Requirements For the Degree of Doctor of Philosophy in Mechanical Engineering College of Engineering and Computing University of South Carolina 2020 Accepted by: Tanvir I. Farouk, Major Professor Bihter Padak, Committee Member Sang Hee Won, Committee Member Jamil A. Khan, Committee Member Cheryl L. Addy, Vice Provost and Dean of the Graduate School © Copyright by Sheikh Farhan Ahmed, 2020 All Rights Reserved ii DEDICATION This thesis is dedicated to my parents whose persistent support and inspiration helped me in every step of my career and worked as magic get through all the difficulties that I faced in the long journey towards this highest academic degree.
    [Show full text]