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Titlebook: Gas Phase Chemical Reaction Systems; Experiments and Mode J. Wolfrum,H.-R. Volpp,J. Warnatz Conference proceedings 1996 Springer-Verlag Ber

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書目名稱Gas Phase Chemical Reaction Systems
副標(biāo)題Experiments and Mode
編輯J. Wolfrum,H.-R. Volpp,J. Warnatz
視頻videohttp://file.papertrans.cn/381/380748/380748.mp4
叢書名稱Springer Series in Chemical Physics
圖書封面Titlebook: Gas Phase Chemical Reaction Systems; Experiments and Mode J. Wolfrum,H.-R. Volpp,J. Warnatz Conference proceedings 1996 Springer-Verlag Ber
描述This volume consists of edited papers presented at the International Symposion Gas Phase Chemical Reaction Systems: Experiments and Models 100 Years After Max Bodenslein, held at the Internationales Wissenschaftsforum Heidelberg (IWH) in Heidelberg during July 25-28, 1995. The intention of this symposion was to bring together leading researchers from the fields of reaction dynamics, kinetics, catalysis and reactive flow model- ling to discuss and review the advances in the understanding of chemical kinetics about 100 years after Max Bodenstein‘s pioneering work on the "hydrogen iodine reaction", which he carried out at the Chemistry Institute of the University of Heidelberg. The idea to focus in his doctoral thesis [1] on this reaction was brought up by his supervisor Victor Meyer (successor of Robert Bunsen at the Chemistry Institute of the University of Heidelberg) and originated from the non- reproducible behaviour found by Bunsen and Roscoe in their early photochemical investigations of the H2/Cl2 system [2] and by van‘t Hoff [3], and V. Meyer and co-workers [4] in their experiments on the slow combustion of H2/02 mixtures.
出版日期Conference proceedings 1996
關(guān)鍵詞Atom; Cross section; Gas-Phase Chemical Reaction Systems; Thermal Kinetics; chemical reaction; cluster; co
版次1
doihttps://doi.org/10.1007/978-3-642-80299-7
isbn_softcover978-3-642-80301-7
isbn_ebook978-3-642-80299-7Series ISSN 0172-6218 Series E-ISSN 2364-9003
issn_series 0172-6218
copyrightSpringer-Verlag Berlin Heidelberg 1996
The information of publication is updating

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Dynamics at Unimolecular Transition Statess above the reaction threshold. These results provide a clear and detailed confirmation of the fundamental hypothesis of the statistical transition state theory (RRKM) that reaction rates are controlled by the number of energetically accessible vibrational levels at the transition state and a striki
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Arbeiter, Unternehmer, Professioneller to investigate in detail the influence of reagent translational excitation on reactivity and reaction dynamics. The experimental results allow comparison with quasiclassical and recent quantum mechanical scattering calculations on . potential energy surfaces.
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https://doi.org/10.1007/978-3-322-89405-2s above the reaction threshold. These results provide a clear and detailed confirmation of the fundamental hypothesis of the statistical transition state theory (RRKM) that reaction rates are controlled by the number of energetically accessible vibrational levels at the transition state and a striki
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Conference proceedings 1996the non- reproducible behaviour found by Bunsen and Roscoe in their early photochemical investigations of the H2/Cl2 system [2] and by van‘t Hoff [3], and V. Meyer and co-workers [4] in their experiments on the slow combustion of H2/02 mixtures.
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