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  • 1
    Online Resource
    Online Resource
    Essen : Inst. f. Physikalische und Theoretische Chemie
    Keywords: Forschungsbericht
    Description / Table of Contents: IO-radical, atmospheric chemistry, ozone depletion
    Type of Medium: Online Resource
    Pages: Online Ressource, 62 p. = 521 Kb., text and images , graphics
    Edition: [Elektronische Ressource]
    Language: German
    Note: Differences between the printed and electronic version of the document are possible. - Contract BMBF 01 LO 9603. - Engl. title: Laboratory studies of the kinetics of stratospheric relevant reactions of IO radicals. - Bibliographic data partially researched , nIndex p. 58 - 62 , Also available as printed version , Systemvoraussetzungen: Acrobat Reader.
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  • 2
    Keywords: Forschungsbericht
    Description / Table of Contents: Radikalanionen, Troposphäre, flüssige Phase, Kinetik, Reaktionssysteme
    Type of Medium: Online Resource
    Pages: 93 p. = 443 kB, text and images
    Edition: [Electronic ed.]
    Language: German
    Note: Contract No.: BMFT/BMBF 07 EU 780 A , nIndex , Differences between the printed and electronic version of the document are possible
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  • 3
    Publication Date: 2019-07-17
    Description: Recent results from kinetic and spectroscopic laboratory studies of reactions of free radicals such as NO3 and SO4- with aromaticcompounds in aqueous solution at T = 298 K are presented. Three different experimental approaches, (i) laser photolysis-visible long-pathlaser absorption, (ii) laser photolysis-UV long-path laser absorption and (iii) time-resolved broadband diode-array spectroscopy, havebeen used to investigate the kinetics of reactions of NO3 and SO4- with aromatics, as well as the formation of oxidation intermediates.For the reactions of NO3 with benzene (1), anisole (2), p-xylene (3), p-cresol (4), toluene (5), mesitylene (6) and 1,4-dimethoxybenzene(7), rate coefficients of k(1) = (4.0 +/- 0.6) x 10(8) 1 mol(-1) s(-1), k(2) = (1.0 +/- 0.4) x 10(9) 1 mol(-1) s(-1), k(3) (1.6 +/- 0.1) x10(9) 1 mol s(-1), k(2) = (1.0 +/- 0.4) x 10(9) mol(-1) 1 s(-1), k(3) = (1.6 +/- 0.1) x 10(9) 1 mol(-1) s(-1), k(4) = (8.4 +/- 2.3) x 10(8)1 mol s(-1) k(5) = (1.2 +/- 0.3) x 10(9) 1 mol(-1) s(-1), k(6) = (1.3 +/- 0.3) x 10(9) 1 mol(-1) s(-1) and k(7) = (1.0 +/- 0.3) x 10(9) 1mol(-1) s(-1) were obtained. For the corresponding reactions of SO4- with benzene (8), toluene (9), p-xylene (10), p-cresol (11) andmesitylene (12), rate coefficients of k(8) = (6.4 +/- 2.5) x 10(8) 1 mol(-1) s(-1), k(9) = (1.3 +/- 0.6) x 10(9) 1 mol(-1) s(-1), k(10) =(2.7 +/- 0.9) x 10(9) 1 mol(-1) s(-1)k(11) = (2.8 +/- 0.8) x 10(9) 1 mol(-1) s(-1) and k(12) = (1.3 +/- 0.4) x 10(9) 1 mol(-1) s(-1) weredetermined. Reactivity correlations for both radical species with the aromatic compounds are presented and potential applications of suchcorrelations are discussed. In addition, the effect of ionic strength in the reactions of NO3 with benzene and toluene has been investigated.Transient intermediates have been spectroscopically identified in the reactions of the sulfate radical anion in aerated as well as inoxygen-free solutions. The nature of these intermediates is discussed in view of the existing literature. Finally, possible impacts offree-radical reactions with aromatic compounds on the current understanding of chemical conversion processes within troposphericmultiphase systems are considered.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 4
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    In:  EPIC3in P. Warneck (Hrsg.), Heterogeneous and liquid phase processes, pp. 146-152
    Publication Date: 2014-04-15
    Repository Name: EPIC Alfred Wegener Institut
    Type: Inbook , peerRev
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  • 5
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    In:  EPIC3Berichte der Bunsen-Gesellschaft - Physical chemistry chemical physics, 101, pp. 1909-1913
    Publication Date: 2019-07-17
    Description: The rate coefficient for the reaction of Cl atoms with (1) H2O and of Cl-2(-) radical anions with (2) H2O and (3) OH- have beendetermined using laser photolysis for the generation of Cl/Cl-2(-) and long path laser absorption for the time resolved detection of Cl-2(-).The following results were obtained: k(1) = (2.3 +/- 0.6).10(5) s(-1), k(2)〈610 s(-1) and k(3) = (4.0+/-0.6).10(6) M-1 s(-1). It isconcluded that the lifetime of Cl/Cl-2(-) in aqueous solution strongly depends on the Cl- content and on pH.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , peerRev
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  • 6
    Publication Date: 2019-07-17
    Description: A Chemical Aqueous Phase Radical Mechanism (CAPRAM) for modelling tropospheric multiphase chemistry is described. CAPRAMcontains (1) a detailed treatment of the oxidation of organic compounds with one and two carbon atoms, (2) an explicit description ofS(IV)-oxidation by radicals and iron(III), as well as by peroxides and ozone, (3) the reactions of OH, NO3, Cl-2(-), Br-2(-), and CO3-radicals, as well as reactions of the transition metal ions (TMI) iron, manganese and copper. A modelling study using a simple box modelwas performed for three different tropospheric conditions (marine, rural and urban) using CAPRAM coupled to the RADM2-mechanism(Stockwell et al., 1990) for liquid and gas phase chemistry, respectively. In the main calculations the droplets are assumed asmonodispersed with a radius of 1 mu m and a liquid water content of 0.3 g m(-3). In the coupled mechanism the phase transfer of 34substances is treated by the resistance model of Schwartz (1989). Results are presented for the concentration levels of the radicals in bothphases under variation of cloud duration and droplet radius.The effects of the multiphase processes are shown in the loss fluxes of the radicals OH, NO3 and HO2 into the cloud droplets. Fromcalculations under urban conditions considering gas phase chemistry only the OH maximum concentration level is found to be 5.5 . 10(6)cm(-3). In the presence of the aqueous phase (r = 1 mu m, LWC = 0.3 g m(-3)) the phase transfer constitutes the most important sink(58%) reducing the OH level to 1.0 . 10(6) cm(-3). The significance of the phase transfer during night time is more important for the NO3radical (90%). Its concentration level in the gas phase (1.9 . 10(9) cm(-3)) is reduced to 1.4 . 10(6) cm(-3) with liquid water present. Inthe case of the HO2 radical the phase transfer from the gas phase is nearly the only sink (99.8%). The concentration levels calculated in theabsence and presence of the liquid phase again differ by three orders of magnitude, 6 . 10(8) cm(-3) and 4.9 . 10(5) cm(-3), respectively.Effects of smaller duration of cloud occurrence and of droplet size variation are assessed.Furthermore, in the present study a detailed description of a radical oxidation chain for sulfur is presented. The most important reactionchain is the oxidation of (hydrogen) sulphite by OH and the subsequent conversion of SO3- to SO5- followed by the interaction with TMI(notably Fe2+) and chloride to produce sulphate. After 36 h of simulation ([H2O2](0) = 1 ppb; [SO2](0) = 10 ppb) the direct oxidationpathway from sulfur(IV) by H2O2 and ozone contributes only to 8% (2.9 . 10(-10) M s(-1)) of the total loss flux of S(IV) (3.7 . 10(-9) Ms(-1)).
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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  • 7
    Publication Date: 2019-07-17
    Description: A laser photolysis-long path laser absorption (LP-LPLA) experiment has been used to determine the rate constants for H-atom abstraction reactions of thedichloride radical anion (Cl2-) in aqueous solution. From direct measurements of the decay of Cl2- in the presence of different reactants at pH = 4 and I = 0.1 M thefollowing rate constants at T = 298 K were derived: methanol, (5.1 ± 0.3)·104 M-1 s-1; ethanol, (1.2 ± 0.2)·105 M-1 s-1; 1-propanol, (1.01 ± 0.07)·105 M-1 s-1;2-propanol, (1.9 ± 0.3)·105 M-1 s-1; tert.-butanol, (2.6 ± 0.5)·104 M-1 s-1; formaldehyde, (3.6 ± 0.5)·104 M-1 s-1; diethylether, (4.0 ± 0.2)·105 M-1 s-1;methyl-tert.-butylether, (7 ± 1)·104 M-1 s-1; tetrahydrofuran, (4.8 ± 0.6)·105 M-1 s-1; acetone, (1.41 ± 0.09)·103 M-1 s-1. For the reactions of Cl2- with formic acidand acetic acid rate constants of (8.0 ± 1.4)·104 M-1 s-1 (pH = 0, I = 1.1 M and T = 298 K) and (1.5 ± 0.8) · 103 M-1 s-1 (pH = 0.42, I = 0.48 M and T = 298K), respectively, were derived.A correlation between the rate constants at T = 298 K for all oxygenated hydrocarbons and the bond dissociation energy (BDE) of the weakest C-H-bond of logk2nd = (32.9 ± 8.9) - (0.073 ± 0.022)·BDE/kJ mol-1 is derived.From temperature-dependent measurements the following Arrhenius expressions were derived:k (Cl2- + HCOOH) = (2.00 ± 0.05)·1010·exp(-(4500 ± 200) K/T) M-1 s-1,Ea = (37 ± 2) kJ mol-1k (Cl2- + CH3COOH) = (2.7 ± 0.5)·1010·exp(-(4900 ± 1300) K/T) M-1 s-1,Ea = (41 ± 11) kJ mol-1k (Cl2- + CH3OH) = (5.1 ± 0.9)·1012·exp(-(5500 ± 1500) K/T) M-1 s-1,Ea = (46 ± 13) kJ mol-1k (Cl2- + CH2(OH)2) = (7.9 ± 0.7)·1010·exp(-(4400 ± 700) K/T) M-1 s-1,Ea = (36 ± 5) kJ mol-1Finally, in measurements at different ionic strengths (I) a decrease of the rate constant with increasing I has been observed in the reactions of Cl2- with methanol andhydrated formaldehyde.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 8
    Publication Date: 2019-07-17
    Description: Nitrate radical (NO3) reactions with benzene (R-1), toluene (R-2), p-xylene (R-3), p-cresol (R-4) and mesitylene (R-5) have beenstudied by laser photolysis/long path laser absorption (LP-LPLA) in aqueous solution. Rate constants of k(1) = (4.0 +/- 0.6) . 10(8), k(2)= (1.2 +/- 0.3) . 10(9), k(3) = (1.6 +/- 0.1) . 10(9), k(4) = (8.4 +/- 2.3) . 10(8) and k(5) = (1.3 +/- 0.3) . 10(9) lmol(-1) s(-1) wereobtained at T = 298 K. In addition, reaction rate coefficients for SO5 + Fe2+ --〉 prod. (R-6) and SO5- + Mn2+ --〉 prod. (R-7) of k(6)= (4.3 +/- 2.4) . 10(7) lmol(-1) s(-1) and k(7) = (4.6 +/- 1.0) . 10(6) lmol(-1) s(-1) (T = 298 K, I --〉 0) have been obtained by theapplication of laser photolysis/UV-VIS broadband diode array spectroscopy. A new laser photolysis/UV-long path laser absorptionexperiment has been applied to study the reaction of the Cl-2(-) radical anion with dissolved sulfur(IV). For the reactions Cl-2(-) +HSO3- --〉 2Cl(-) + H+ + SO3- (R-8) and Cl-2(-) + SO32- --〉 2Cl(-) + SO3- (R-9) rate coefficients of k(8) = (1.7 +/- 0.2) . 10(8)lmol(-1) s(-1) (T = 298 K, I --〉 0) and of k(9) = (6.2 +/- 0.3) . 10(7) lmol(-1) s(-1) (T = 279 K, I --〉 0) were obtained.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 84 (1980), S. 3196-3198 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 88 (1984), S. 984-989 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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