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The role of water vapor (H2O) and its hydrogen-bonded complexes in the gas-phase reactivity of organic compounds with hydroxyl (OH) radicals has been the subject of many recent studies. Contradictory effects have been reported at temperatures between 200 and 400 K. For the OH + acetaldehyde reaction, a slight catalytic effect of H2O was previously reported at temperatures between 60 and 118 K. In this work, we used Laval nozzle expansions to reinvestigate the impact of H2O on the OH-reactivity with acetaldehyde between 21.7 and 135.0 K. The results of this comprehensive study demonstrate that water, instead, slows down the reaction by factors of â¼3 (21.7 K) and â¼2 (36.2-89.5 K), and almost no effect of added H2O was observed at 135.0 K.
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Ethanol, CH3CH2OH, has been unveiled in the interstellar medium (ISM) by radioastronomy and it is thought to be released into the gas phase after the warm-up phase of the grain surface, where it is formed. Once in the gas phase, it can be destroyed by different reactions with atomic and radical species, such as hydroxyl (OH) radicals. The knowledge of the rate coefficients of all these processes at temperatures of the ISM is essential in the accurate interpretation of the observed abundances. In this work, we have determined the rate coefficient for the reaction of OH with CH3CH2OH (k(T)) between 21 and 107 K by employing the pulsed and continuous CRESU (Cinétique de Réaction en Ecoulement Supersonique Uniforme, which means Reaction Kinetics in a Uniform Supersonic Flow) technique. The pulsed laser photolysis technique was used for generating OH radicals, whose time evolution was monitored by laser induced fluorescence. An increase of approximately 4 times was observed for k(21 K) with respect to k(107 K). With respect to k(300 K), the OH-reactivity at 21 K is enhanced by two orders of magnitude. The obtained T-expression in the investigated temperature range is k(T) = (2.1 ± 0.5) × 10-11 (T/300 K)-(0.71±0.10) cm3 molecule-1 s-1. In addition, the pressure dependence of k(T) has been investigated at several temperatures between 21 K and 90 K. No pressure dependence of k(T) was observed in the investigated ranges. This may imply that this reaction is purely bimolecular or that the high-pressure limit is reached at the lowest total pressure experimentally accessible in our system. From our results, k(T) at usual IS temperatures (â¼10-100 K) is confirmed to be very fast. Typical rate coefficients can be considered to range within about 4 × 10-11 cm3 molecule-1 s-1 at 100 K and around 1 × 10-10 cm3 molecule-1 s-1 at 20 K. The extrapolation of k at the lowest temperatures of the dense molecular clouds of ISM is also discussed in this paper.
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The article "Methanol dimer formation drastically enhances hydrogen abstraction from methanol by OH at low temperature" proposes a dimer mediated mechanism in order to explain the large low temperature rate coefficients for the OH + methanol reaction measured by several groups. It is demonstrated here theoretically that under the conditions of these low temperature experiments, there are insufficient dimers formed for the proposed new mechanism to apply. Experimental evidence is also presented to show that dimerization of the methanol reagent does not influence the rate coefficients reported under the conditions of methanol concentration used for the kinetics studies. It is also emphasised that the low temperature experiments have been performed using both the Laval nozzle expansion and flow-tube methods, with good agreement found for the rate coefficients measured using these two distinct techniques.
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The gas phase chemistry of neutral-neutral reactions of interest in the interstellar medium (ISM) is poorly understood. The rate coefficients (kOH) for the majority of the reactions of hydroxyl (OH) radicals with interstellar oxygenated species are unknown at the temperatures of the ISM. In this study, we present the first determination of kOH for HC(O)OCH3 between 22.4 ± 1.4 and 64.2 ± 1.7 K. The CRESU (French acronym for Cinétique de Réaction en Ecoulement Supersonique Uniforme or Reaction Kinetics in a Uniform Supersonic Flow) technique was used to create a chemical reactor with a uniform temperature and gas density and the pulsed laser photolysis/laser induced fluorescence technique was used to generate OH radicals and to monitor their temporal profile. It was observed that kOH(T) increases by one order of magnitude in only â¼40 K (kOH(T = 22 K) = (1.19 ± 0.36) × 10(-10) cm(3) s(-1) and kOH(T = 64 K) = (1.16 ± 0.12) × 10(-11) cm(3) s(-1)) and â¼3 orders of magnitude with respect to kOH(T = 298 K). This reaction is a very efficient route for the loss of HC(O)OCH3 in the gas phase and may have a great impact on the interpretation of astrophysical models of HC(O)OCH3 abundance in the cold regions of the ISM.
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Three different detection techniques, coupled to pulsed laser photolysis (PLP), have been employed to determine the quantum yields of CF3CH2CHO at 248 and 266 nm: CF3CH2CHO + hν â CF3CH2 + HCO (R1a), CF3CH2CHO + hν â CF3CH3 + CO (R1b), and CF3CH2CHO + hν â CF3CH2O + H (R1c). (a) In the presence of air, Fourier transform infrared (FTIR) spectroscopy was employed at a total pressure of 760 Torr to monitor and quantify the loss of CF3CH2CHO at both wavelengths as well as the build-up of formed products (CO, CF3CH3, CF3CHO, and CF3CH2OH) after various laser pulses. Cyclohexane was added as OH-scavenger in most experiments. CF3CH3 was observed and quantified at both wavelengths, confirming that channel R1b is occurring. Small amounts of HCOOH and COF2 were also detected. (b) Time-resolved cw-cavity ring down spectroscopy (cw-CRDS) at 40 Torr He coupled to photolysis at 248 nm was employed for the detection of HO2 radicals. Varying the O2 concentration allows distinguishing the origin of the HO2 radicals from either R1a or R1c. OH radicals were simultaneously detected by laser-induced fluorescence. (c) Time-resolved tunable diode laser absorption spectroscopy (TDLAS) at 30 Torr N2 coupled to photolysis at 266 nm was employed for the determination of the quantum yields of CO. By varying the O2 concentration, a distinction can be achieved between the yields of prompt CO R1b or decomposition of highly excited CF3CH2CO from R1c and HCO radicals R1a. Channel R1a has been identified as the major reaction path. The overall quantum yield, Φλ(CF3CH2CHO), at 248 nm was found as Φ248nm = (0.76 ± 0.14) and (0.73 ± 0.20) from cw-CRDS and FTIR experiments, respectively. At 266 nm, the overall quantum yield was found as Φ266nm = (0.55 ± 0.10) and (0.47 ± 0.10) from TDLAS and FTIR experiments, respectively.
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The relative-rate technique has been used to determine the rate coefficient for the reaction of CxF2x+1CHCH2 (xâ¯=â¯1, 2, 3, 4 and 6) with ozone at (298⯱â¯2) K and (720⯱â¯5) Torr of air by FTIR (Fourier Transform Infrared Spectroscopy) and by GC-MS/SPME (Gas Chromatography-Mass Spectroscopy with Solid Phase Micro Extraction) in two different atmospheric simulation chambers. The following rate coefficients, in units of 10-19â¯cm3 molecule-1 s-1, were obtained: (3.01⯱â¯0.10) for CF3CHCH2, (2.11⯱â¯0.35) for C2F5CHCH2, (2.34⯱â¯0.42) for C3F7CHCH2, (2.05⯱â¯0.31) for C4F9CHCH2 and (2.07⯱â¯0.39) for C6F13CHCH2, where uncertainties represent ±2σ statistical error. The atmospheric lifetime of CxF2x+1CHCH2 due to reaction with ozone was estimated from the reported rate coefficients. Additionally, the gaseous products formed in these reactions were investigated in the presence of synthetic air simulating a clean atmosphere. Perfluoroaldehydes, CxF2x+1C(O)H (PFALs), formaldehyde, formic acid and CF2O were identified as reaction products in the investigated reactions. The identified products made possible to propose a reaction mechanism that justifies the observed products. The atmospheric implications of these results are discussed in terms of the potential contribution of the atmospheric degradation of these species to PFAL and PFCA burden.
Assuntos
Atmosfera/química , Gases/química , Hidrocarbonetos Fluorados/química , Ozônio/química , Fluorocarbonos/química , Cromatografia Gasosa-Espectrometria de Massas , Radical Hidroxila/química , Cinética , Microextração em Fase Sólida , Espectroscopia de Infravermelho com Transformada de FourierRESUMO
Unsaturated ethers are oxygenated volatile organic compounds (OVOCs) emitted by anthropogenic sources. Potential removal processes in the troposphere are initiated by hydroxyl (OH) radicals and photochemistry. In this work, we report for the first time the rate coefficients of the gas-phase reaction with OH radicals (kOH) of 2-chloroethyl vinyl ether (2ClEVE), allyl ether (AE), and allyl ethyl ether (AEE) as a function of temperature in the 263-358 K range, measured by the pulsed laser photolysis-laser induced fluorescence technique. No pressure dependence of kOH was observed in the 50-500 Torr range in He as bath gas, while a slightly negative T-dependence was observed. The temperature dependent expressions for the rate coefficients determined in this work are: The estimated atmospheric lifetimes (τOH) assuming kOH at 288 K were 3, 2, and 4 h for 2ClEVE, AE and AEE, respectively. The kinetic results are discussed in terms of the chemical structure of the unsaturated ethers by comparison with similar compounds. We also report ultraviolet (UV) and infrared (IR) absorption cross sections (σλ and σ(νË), respectively). We estimate the photolysis rate coefficients in the solar UV actinic region to be less than 10-7 s-1, implying that these compounds are not removed from the atmosphere by this process. In addition, from σ(νË) and τOH, the global warming potential of each unsaturated ether was calculated to be almost zero. A discussion on the atmospheric implications of the titled compounds is presented.
Assuntos
Atmosfera/química , Éteres/química , Fotoquímica/métodos , Aquecimento Global , Radical Hidroxila/química , Cinética , Fotólise , Pressão , Luz Solar , TemperaturaRESUMO
Chemical kinetics of neutral-neutral gas-phase reactions at ultralow temperatures is a fascinating research subject with important implications on the chemistry of complex organic molecules in the interstellar medium (Tâ¼10-100K). Scarce kinetic information is currently available for this kind of reactions at T<200 K. In this work we use the CRESU (Cinétique de Réaction en Ecoulement Supersonique Uniforme, which means Reaction Kinetics in a Uniform Supersonic Flow) technique to measure for the first time the rate coefficients (k) of the gas-phase OH+H2CO reaction between 22 and 107 K. k values greatly increase from 2.1×10-11 cm3 s-1 at 107 K to 1.2×10-10 cm3 s-1 at 22 K. This is also confirmed by quasi-classical trajectories (QCT) at collision energies down to 0.1 meV performed using a new full dimension and ab initio potential energy surface, recently developed which generates highly accurate potential and includes long range dipole-dipole interactions. QCT calculations indicate that at low temperatures HCO is the exclusive product for the OH+H2CO reaction. In order to revisit the chemistry of HCO in cold dense clouds, k is reasonably extrapolated from the experimental results at 10K (2.6×10-10 cm3 s-1). The modeled abundances of HCO are in agreement with the observations in cold dark clouds for an evolving time of 105-106 yrs. The different sources of production of HCO are presented and the uncertainties in the chemical networks discussed. This reaction can be expected to be a competitive process in the chemistry of prestellar cores. The present reaction is shown to account for a few percent of the total HCO production rate. Extensions to photodissociation regions and diffuse clouds environments are also commented.
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In the last years, ultra-low temperature chemical kinetic experiments have demonstrated that some gas-phase reactions are much faster than previously thought. One example is the reaction between OH and CH3OH, which has been recently found to be accelerated at low temperatures yielding CH3O as main product. This finding opened the question of whether the CH3O observed in the dense core Barnard 1b could be formed by the gas-phase reaction of CH3OH and OH. Several chemical models including this reaction and grain-surface processes have been developed to explain the observed abundance of CH3O with little success. Here we report for the first time rate coefficients for the gas-phase reaction of OH and CH3OH down to a temperature of 22 K, very close to those in cold interstellar clouds. Two independent experimental set-ups based on the supersonic gas expansion technique coupled to the pulsed laser photolysis-laser induced fluorescence technique were used to determine rate coefficients in the temperature range 22-64 K. The temperature dependence obtained in this work can be expressed as k(22-64 K) = (3.6 ± 0.1) × 10-12(T/300 K)-(1.0±0.2) cm3 molecule-1 s-1. Implementing this expression in a chemical model of a cold dense cloud results in CH3O/CH3OH abundance ratios similar or slightly lower than the value of â¼ 3 × 10-3 observed in Barnard 1b. This finding confirms that the gas-phase reaction between OH and CH3OH is an important contributor to the formation of interstellar CH3O. The role of grain-surface processes in the formation of CH3O, although it cannot be fully neglected, remains controversial.